BOC Sciences provides a wide range of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
| Product | Description | |
|---|---|---|
| 3'-O-Acetyl-2'-deoxyguanosine | 3'-O-Acetyl-2'-deoxyguanosine is a derivative of deoxyguanosine, exhibiting intricate modifications. Its utilization primarily lies in the study of nucleotide analogs and nucleoside chemistry, enabling the research of groundbreaking antiviral medications. Moreover, it serving as a potent tool in exploring the intricate interplay between acetylation, nucleoside metabolism is and cellular functions. Synonyms: 3'-O-Ac-dG; 2'-Deoxyguanosine 3'-acetate; 2'-deoxy-3'-O-acetylguanosine; 2-Amino-9-(3-O-acetyl-2-deoxy-β-D-ribofuranosyl)-9H-purin-6(1H)-one. Grade: ≥98% by HPLC. CAS No. 51549-58-7. Molecular formula: C12H15N5O5. Mole weight: 309.28. |  |
| 3'-(O-acetyl)-2'-deoxyguanosine (N-iBu) | 3'-(O-acetyl)-2'-deoxyguanosine (N-iBu) is an esteemed biomedical compound, manifesting unprecedented aptitude in thwarting cancer cell proliferation and impeding their egregious expansion. Grade: ≥ 98% by HPLC. Molecular formula: C16H21N5O6. Mole weight: 379.37. | |
| 3'-O-Acetyl-2'-deoxy-N2-isobutyrylguanosine | 3'-O-Acetyl-2'-deoxy-N2-isobutyrylguanosine, a remarkable biomedicine, holds immense potential for combating specific viral infections and cancers. Its profound antiviral and anticancer properties stem from its remarkable capacity to impede viral DNA replication and restrict tumor proliferation. With extensive presence across diverse chemical databases, this compound prominently assists in the progressive research and development of pharmaceutical ventures targeting these complex diseases. Synonyms: 2'-Deoxy-N-(2-methyl-1-oxopropyl)?-guanosine 3'-acetate. Grade: 99%. CAS No. 74925-81-8. Molecular formula: C16H21N5O6. Mole weight: 379.37. | |
| 3'-(O-acetyl)-2'-deoxythymidine | 3'-(O-acetyl)-2'-deoxythymidine is a vital compound widely used in the biomedical industry playing a crucial role in the reserch of viral diseases, particularly HIV. This compound exhibits antiviral properties and is used as a key component in the development of antiretroviral drugs. Its ability to inhibit viral replication makes it an essential tool in research of HIV and other related infections. Grade: ≥ 98% by HPLC. Molecular formula: C12H16N2O6. Mole weight: 284.27. | |
| 3'-(O-acetyl)-2'-deoxyuridine | 3'-(O-acetyl)-2'-deoxyuridine, also known as acetyldeoxyuridine, is a multifaceted nucleoside analog extensively employed in the field of biomedical research and drug development. It exhibits remarkable prospects in the realm of cancer reserch by impeding DNA research and development and inducing apoptosis in malignant neoplastic cells. Grade: ≥ 98% by HPLC. Molecular formula: C11H14N2O6. Mole weight: 270.24. | |
| 3-O-Acetyl-4-O-methyl-D-glucuronic acid | 3-O-Acetyl-4-O-methyl-D-glucuronic acid is a noteworthy chemical entity used in studying multifarious ailments like carcinoma, diabetes mellitus and inflammatory conditions. CAS No. 2892629-39-7. Molecular formula: C9H14O8. Mole weight: 250.20. | |
| 3'-O-Acetyl-4'-thio-2'-deoxy-beta-D-uridine | 3'-O-Acetyl-4'-thio-2'-deoxy-β-D-uridine is a modified uridine nucleoside where the 3' hydroxyl group is protected with an acetyl group, and the 4' position of the sugar is modified by replacing the oxygen atom with a sulfur atom (creating a thionucleoside). Additionally, the sugar is 2'-deoxyribose, which is characteristic of DNA nucleosides. This compound is likely used in specialized nucleic acid synthesis, such as creating modified RNA or DNA analogs. The protective groups and sulfur substitution can influence the reactivity, stability, and incorporation of this nucleoside in oligonucleotide synthesis, potentially providing insights into biochemical interactions or therapeutic applications. Synonyms: 1-[2-Deoxy-3-o-acetyl-4-thio-beta-d-ribofuranosyl]uracil; Uridine, 2'-deoxy-4'-thio-, 3'-acetate; 3'-O-Acetyl-2'-Deoxy-4'-thiouridine; (2R,3S,5R)-5-(2,4-Dioxo-3,4-dihydropyrimidin-1(2H)-yl)-2-(hydroxymethyl)tetrahydrothiophen-3-yl acetate. Grade: ≥95%. CAS No. 667882-69-1. Molecular formula: C11H14N2O5S. Mole weight: 286.31. | |
| 3'-O-Acetyl-5-Benzylaminocarbonyl-5'-O-DMT-2'-O-methyluridine | 3'-O-Acetyl-5-Benzylaminocarbonyl-5'-O-DMT-2'-O-methyluridine, a synthetic nucleoside derivative, has been the subject of extensive research for its potential applications in the treatment of viral infections, including hepatitis C and HIV, as well as cancer chemotherapy. With its unique molecular structure, this compound shows great promise in the development of effective antiviral agents. Moreover, its potential uses in cancer treatment suggest it may represent a major breakthrough in the fight against this deadly disease. Synonyms: 5-Benzylaminocarbony-3'-O-acetyl-2'-O-methyl-5'-O-DMTr-uridine; 5-Benzylaminocarbony-3'-O-acetyl-2'-O-methyl-5'-O-(4,4'-dimethoxytrityl)uridine. Grade: ≥95%. CAS No. 2095417-22-2. Molecular formula: C41H41N3O10. Mole weight: 735.78. | |
| 3'-O-Acetyl-5'-Des(hydroxymethyl)-5'-carboxymethyl Decitabine | 3'-O-Acetyl-5'-Des(hydroxymethyl)-5'-carboxymethyl Decitabine is an impurity of Decitabine, which is a potent inhibitor of DNA methylation. Synonyms: (2S,3S,5R)-2-Acetyl-5-(4-amino-2-oxo-1,3,5-triazin-1(2H)-yl)tetrahydrofuran-3-yl Acetate. Molecular formula: C11H14N4O5. Mole weight: 282.25. | |
| 3'-O-Acetyl-5'-O-DMT-2'-O-methyl-5-naphthyl-b-methylaminocarbonyl-uridine | Modified uridine, 3'-O-Acetyl-5'-O-DMT-2'-O-methyl-5-naphthyl-b-methylaminocarbonyl-uridine, is a vital component in biomedicine research. Its application is typically directed towards nucleotide analogs creation, particularly in the fight against hepatitis C and HIV. Its impact in antiviral therapy is unequivocal, and as such, commands utmost attention in scientific research. Synonyms: 5-Naphthyl-beta-methylaminocarbony-3'-O-acetyl-2'-O-methyl-5'-O-DMTr-uridine. Grade: ≥95%. CAS No. 2095417-00-6. Molecular formula: C45H43N3O10. Mole weight: 785.84. | |
| 3'-O-Acetyl-5'-O-DMT-2'-O-methyuridine | 3'-O-Acetyl-5'-O-DMT-2'-O-methyuridine, a modified uridine nucleoside, has garnered significant attention in the fields of gene therapy and oncology due to its potential as a potent RNA molecule developer for gene silencing and regulation. Extensive research has shown promising results, suggesting that this compound has the ability to selectively target genes and inhibit protein production, thereby presenting an intriguing therapeutic avenue for diseases. Molecular formula: C33H34N2O9. Mole weight: 602.63. | |
| 3'-O-Acetyl-5'-O-DMT-5-iodo-2'-O-methyl-uridine | Highly specialized in the field of biomedicine, 3'-O-Acetyl-5'-O-DMT-5-iodo-2'-O-methyl-uridine stands as a critical compound. Its employment primarily revolves around synthesizing nucleotide analogs for antiviral drug development and acting as a probe in biochemical studies concerning RNA. Promising therapeutic applications against viral infections, like HIV and hepatitis B, are attributed to this product. Synonyms: 5'-O-(4,4'-dimethoxytrityl)-3'-acetyl-5-Iodo-2'-O-methyl-uridine; 5'-O-DMT-3'-Ac-5-I-2'-OMe-Ur; 5'-O-(4,4'-Dimethoxytrityl)-2'-O-methyl-3'-O-acetyl-5-iodouridine; 5'-O-[Bis(4-methoxyphenyl)?phenylmethyl]?-5-iodo-2'-O-methyl-uridine 3'-acetate; 5-Iodo-5'-DMT-2'-O-methyl-3'-acetyl-uridine; 3'-O-Acetyl-5'-O-[bis(4-methoxyphenyl)(phenyl)methyl]-5-iodo-2'-O-methyluridine. Grade: ≥95%. CAS No. 1374692-34-8. Molecular formula: C33H33IN2O9. Mole weight: 728.53. | |
| 3'-O-Acetyl-5'-O-tert-butyldiphenylsilyl-2'-deoxy-2'-fluorothymidine | 3'-O-Acetyl-5'-O-tert-butyldiphenylsilyl-2'-deoxy-2'-fluorothymidine, possessing immense significance in the field of biomedicine, serves as a pivotal entity. Renowned for its remarkable application as an antiviral agent against Human Immunodeficiency Virus (HIV) infections, with a specific focus on inhibiting reverse transcriptase, this compound assumes a paramount role. Synonyms: 3'-O-Acetyl-5'-O-tert-butyldiphenylsilyl-2'-deoxy-2'-fluoro-D-thymidine. Molecular formula: C28H33FN2O6Si. Mole weight: 540.66. | |
| 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose | 3-O-Acetyl-6-O-benzoyl-5-O-methylsulfonyl-1,2-O-isopropylidene-a-D-glucofuranose is a biomedical product used in the research of certain diseases and conditions. This compound has potential applications as an antiviral and antifungal agent. It can also be utilized as a chemical intermediate in the synthesis of pharmaceutical drugs targeting specific diseases, due to its unique structural properties. CAS No. 102029-58-3. Molecular formula: C19H24O10S. Mole weight: 444.45. | |
| 3-O-Acetyl Ezetimibe | An impurity of Ezetimibe. Ezetimibe inhibits intestinal cholesterol absorption by preventing cholesterol uptake by the Niemann-Pick C1-like 1 (NPC1L4) protein, a cholesterol transporter located in the apical membrane of enterocytes. Synonyms: (3R,4S)- 3-[(3S)-3-(acetyloxy)-3-(4-fluorophenyl)propyl]-1-(4-fluorophenyl)-4-(4-hydroxyphenyl)-2-Azetidinone. Grade: > 95%. CAS No. 190448-46-5. Molecular formula: C26H23F2NO4. Mole weight: 451.47. | |
| 3-O-Acetyl ezetimibe 2,3,4-tri-o-acetyl-β-D-glucuronide methyl ester | An intermediate of Ezetimibe. Ezetimibe is a selective cholesterol absorption inhibitor that targets the Niemann-Pick C1-Like 1 (NPC1L1) protein in the small intestine, blocking dietary and biliary cholesterol uptake. Uses: Intermediate in the preparation of phase-ii metabolites of ezetimibe. glucuronide azetidinone cholesterol absorption inhibitor. Synonyms: β-D-Glucopyranosiduronic acid, 4-[(2S,3R)-3-[(3S)-3-(acetyloxy)-3-(4-fluorophenyl)propyl]-1-(4-fluorophenyl)-4-oxo-2-azetidinyl]phenyl, methyl ester, 2,3,4-triacetate; 4-[(2S,3R)-3-[(3S)-3-(Acetyloxy)-3-(4-fluorophenyl)propyl]-1-(4-fluorophenyl)-4-oxo-2-azetidinyl]phenyl β-D-Glucopyranosiduronic Acid Methyl Ester 2,3,4-Triacetate. Grade: ≥95%. CAS No. 190448-56-7. Molecular formula: C39H39F2NO13. Mole weight: 767.72. | |
| 3'-O-Acetyl-N2-isobutyryl-4'-thio-2'-deoxy-beta-D-guanosine | 3'-O-Acetyl-N2-isobutyryl-4'-thio-2'-deoxy-β-D-guanosine is a chemically modified nucleoside with multiple functional group modifications. The 3'-hydroxyl group of the deoxyribose sugar is acetylated, and the N2 position of the guanine base is protected with an isobutyryl group. Additionally, the 4'-oxygen atom of the sugar is replaced by sulfur, forming a 4'-thio sugar derivative. The acetyl and isobutyryl groups act as protecting groups during oligonucleotide synthesis, ensuring selective reactions at other sites. This compound is primarily used in nucleic acid chemistry for synthesizing modified oligonucleotides, offering enhanced stability, nuclease resistance, and unique structural or biochemical properties for research or therapeutic applications. Synonyms: N-(2-Methyl-1-oxopropyl)-3'-O-acetyl-2'-deoxy-4'-thioguanosine; N2-Isobutyryl-3'-O-acetyl-4'-thio-2'-deoxyguanosine. Molecular formula: C16H21N5O5S. Mole weight: 395.43. | |
| 3'-O-Acetyl-N4-acetyl-4'-thio-2'-deoxy-beta-D-cytidine | 3'-O-Acetyl-N4-acetyl-4'-thio-2'-deoxy-beta-D-cytidine is a modified nucleoside with multiple structural changes. The 3'-O-acetyl group is attached to the 3' hydroxyl group of the sugar, which can protect the molecule from exonuclease degradation and contribute to stability. The N4-acetyl group is attached to the N4 position of the cytosine base, potentially altering the interactions of the nucleoside with other nucleic acids or proteins. The 4'-thio modification replaces the oxygen atom at the 4' position of the sugar with a sulfur atom, which enhances stability and can increase binding affinity. The 2'-deoxy structure means the nucleoside lacks the 2'-hydroxyl group, making it a deoxyribonucleotide and suitable for DNA synthesis. This modified nucleoside can be used in the synthesis of DNA oligonucleotides, especially for applications requiring enhanced stability, altered enzyme interactions, or resistance to degradation. Synonyms: Cytidine, N-acetyl-2'-deoxy-4'-thio-, 3'-acetate; N-Acetyl-2'-deoxy-3'-O-acetyl-4'-thio-cytidine; N4-Acetyl-2'-deoxy-3'-O-acetyl-4'-thio-cytidine. Molecular formula: C13H17N3O5S. Mole weight: 327.36. | |
| 3'-O-Acetyl-N4-benzoyl-4'-thio-2'-deoxy-beta-D-cytidine | 3'-O-Acetyl-N4-benzoyl-4'-thio-2'-deoxy-beta-D-cytidine is a modified nucleoside with several structural modifications. The 3'-O-acetyl group is attached to the 3' hydroxyl of the sugar, providing steric protection and increasing the stability of the nucleoside. The N4-benzoyl modification is attached to the nitrogen at the N4 position of the cytosine base, which can affect its interactions with other nucleic acids or enzymes, potentially enhancing binding affinity or altering recognition. The 4'-thio modification replaces the oxygen atom at the 4' position of the ribose sugar with a sulfur atom, which can increase the stability and binding affinity of the nucleoside. The 2'-deoxy structure indicates the absence of the 2'-hydroxyl group, making it a deoxyribonucleotide, suitable for DNA synthesis. This modified nucleoside can be used in DNA research, gene editing, or therapeutic applications where increased stability, nuclease resistance, and specific interactions with biological targets are important. Synonyms: Cytidine, N-benzoyl-2'-deoxy-4'-thio-, 3'-acetate; N-Benzoyl-2'-deoxy-3'-O-acetyl-4'-thio-cytidine; N4-Benzoyl-2'-deoxy-3'-O-acetyl-4'-thio-cytidine. Grade: ≥95%. CAS No. 667882-71-5. Molecular formula: C18H19N3O5S. Mole weight: 389.43. | |
| 3'-O-Acetyl-N6-benzoyl-4'-thio-2'-deoxy-beta-D-adenosine | 3'-O-Acetyl-N6-benzoyl-4'-thio-2'-deoxy-beta-D-adenosine is a modified nucleoside with several structural changes. The 3'-O-acetyl group is attached to the 3' position of the sugar, providing steric protection and increasing the stability of the nucleoside. The N6-benzoyl modification is attached to the adenine base at the N6 position, which can alter the interactions of the nucleoside with enzymes or other nucleic acids. The 4'-thio modification involves replacing the oxygen at the 4' position of the sugar with a sulfur atom, which can enhance the stability and binding properties of the nucleoside. Finally, the 2'-deoxy structure indicates the absence of the hydroxyl group at the 2' position, making it a deoxyribonucleotide. This modified nucleoside can be used in DNA synthesis, particularly for research applications involving stability enhancement, resistance to nucleases, and altered interactions with biological systems. Synonyms: Adenosine, N-benzoyl-2'-deoxy-4'-thio-, 3'-acetate; N-Benzoyl-2'-deoxy-3'-O-acetyl-4'-thioadenosine; N6-Benzoyl-2'-deoxy-3'-O-acetyl-4'-thioadenosine. Grade: ≥95%. CAS No. 667882-73-7. Molecular formula: C19H19N5O4S. Mole weight: 413.45. | |
| 3'-O-Acetylthymidine | 3'-O-Acetylthymidine is a widely utilized biomedical compound, exhibiting its prowess in research of specific viral infections and cancer. Serving as a formidable nucleoside analog, it unleashes its latent potential as a potent antiviral and antitumor agent. Synonyms: 3'-O-Ac-dT; 3'-O-Acetyl-D-thymidine; (2R,3S,5R)-2-(Hydroxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3-yl acetate; Thymidine, 3'-acetate. Grade: ≥98% by HPLC. CAS No. 21090-30-2. Molecular formula: C12H16N2O6. Mole weight: 284.27. | |
| 3-O-(a-D-Galactopyranosyl)-b-D-fucopyranosyl propylamine | 3-O-(a-D-Galactopyranosyl)-b-D-fucopyranosyl propylamine is a compound with potential anti-tumor properties. It has been researched as a potential drug candidate for the treatment of ovarian, breast and prostate cancer. Initial studies have shown that it can inhibit the growth and proliferation of cancer cells by inducing apoptosis. Synonyms: Gala3FucbOCH2CH2CH2NH2. Molecular formula: C15H29NO10. Mole weight: 383.39. | |
| 3-O-(a-D-Galactopyranosyl)-D-galactose | 3-O-(a-D-Galactopyranosyl)-D-galactose is a crucial compound used in biomedicine for its potential in treating specific disorders. This product exhibits promising therapeutic effects in managing various diseases involving galactose metabolism dysfunction or defective glycoprotein biosynthesis, such as glycosylation disorders, galactosemia, and certain liver diseases. Synonyms: 3-O-α-D-Galactopyranosyl-D-galactose; Galα1-3Gal; α1-3 Galactobiose; Gal-a-1,3-Gal; alpha-D-galactosyl-(1->3)-D-galactose; 3α-Galactobiose; α-D-Galp-(1-3)-D-Gal; 3-O-alpha-D-Galactosylgalactose. Grade: ≥95%. CAS No. 13168-24-6. Molecular formula: C12H22O11. Mole weight: 342.30. | |
| 3-O-(a-D-Mannopyranosyl)-D-mannopyranose | It is an inhibitor of fimbrial lectins from enterobacteria. Synonyms: 3-O-(α-D-Mannopyranosyl)-D-mannopyranose; α1-3 Mannobiose; Man-a-1,3-Man; 3α-Mannobiose; alpha-D-Man-(1->3)-D-Man; alpha-D-Manp-(1->3)-D-Manp; alpha-D-Mannosyl-(1->3)-D-mannose; 3-O-α-D-Mannopyranosyl-D-mannopyranose; Mannopyranose, 3-O-α-D-mannopyranosyl-, D-; α-1,3-Mannobiose. Grade: ≥95%. CAS No. 23745-85-9. Molecular formula: C12H22O11. Mole weight: 342.30. | |
| 3-O-(a-D-Mannopyranosyl)-D-mannopyranose 1-O-propylamine acetate salt | 3-O-(a-D-Mannopyranosyl)-D-mannopyranose 1-O-propylamine acetate salt is a highly intricate compound, having the potential to thwart tumor cells growth. Not only that, it showcases remarkable antiviral attributes in the research of viruses like Zika and dengue. Synonyms: Mana1-3-mana1-O-propylamine acetate; D-Mannopyranoside, 3-aminopropyl 3-O-α-D-mannopyranosyl-, acetate (1:1); 3-Aminopropyl 3-O-α-D-mannopyranosyl-D-mannopyranoside, acetate. Grade: 90%. Molecular formula: C17H33O13N. Mole weight: 459.44. | |
| 3-O-(a-D-Mannopyranosyl)-D-mannose | 3-O-(a-D-Mannopyranosyl)-D-mannose, named as α-Mannan, is an indispensable element within the biomedical realm. Renowned for its immunomodulatory and anti-inflammatory properties, this magical compound assumes a pivotal role in the therapeutic arsenal against a multitude of ailments, encompassing allergies, autoimmune disorders, and chronic inflammation. By deftly orchestrating immune responses and curbing unwarranted inflammation, this marvel affords respite to afflicted individuals, emancipating them from the clutches of these tormenting afflictions. Synonyms: 1,3-Mannosylmannose; Manalpha1-3Man; 3-O-α-D-Mannopyranosyl-D-mannose; Mannose, 3-O-α-D-mannopyranosyl-, D-; 3α-Mannobiose; α-D-Man-(1→3)-D-Man. CAS No. 34141-02-1. Molecular formula: C12H22O11. Mole weight: 342.30. | |
| 3-O-(a-L-Fucopyranosyl)-4-O-(3-sialyl-b-D-galactopyranosyl)-D-glucose | 3-O-(α-L-Fucopyranosyl)-4-O-(3-sialyl-β-D-galactopyranosyl)-D-glucose is a remarkable compound, intriguingly elucidating the intricacies encompassing cellular recognition and signal transduction, particularly concerning carbohydrates. Synonyms: Neu5Ac-a-2,3-Gal-b-1,4(Fuca1,3)Glc. Molecular formula: C29H51NO22. Mole weight: 765.71. | |
| 3-O-(a-L-Fucopyranosyl)-b-D-galactopyranose | 3-O-(a-L-Fucopyranosyl)-b-D-galactopyranose, commonly known as Fuc-Gal, is a significant biomolecule widely utilized in the realm of biomedical research. This compound serves as an essential substrate for the enzymes engaged in intricate glycosylation processes, thereby facilitating the synthesis of glycoproteins. Its pivotal role in elucidating abnormal glycosylation patterns associated with diverse conditions like cancer, genetic disorders, and immune system aberrations cannot be overstated. Synonyms: Fuca1-3Gal; 3-O-(6-Deoxy-α-L-galactopyranosyl)-β-D-galactopyranose; Fuc(a1-3)b-Gal. CAS No. 120375-11-3. Molecular formula: C12H22O10. Mole weight: 326.30. | |
| 3-O-Allyl-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose | 3-O-Allyl-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose. Synonyms: 1,2:5,6-Di-O-isopropylidene-3-O-2-propen-1-yl-α-D-glucofuranose; 1,2:5,6-bis-O-(1-Methylethylidene)-3-O-2-propen-1-yl-α-D-glucofuranose. CAS No. 20316-77-2. Molecular formula: C15H24O6. Mole weight: 300.35. | |
| 3-O-Allyl-1,2-O-isopropylidene-a-D-galactofuranose | 3-O-Allyl-1,2-O-isopropylidene-α-D-galactofuranose is a compound ingredient utilized in the development of drugs targeting various diseases. This compound's unique structure and properties make it a valuable tool for researchers in the biomedical industry aiming to design innovative research for these conditions. CAS No. 1423018-05-6. Molecular formula: C12H20O6. Mole weight: 260.28. | |
| 3'-O-Allyl-2'-deoxyadenosine | 3'-O-Allyl-2'-deoxyadenosine, a formidable antiviral agent, is primed to revolutionize the realm of viral therapeutics. Its potency transcends beyond the confines of HIV, herpes simplex virus, and hepatitis B virus, executing ailing viruses with precision. By obstructing viral replication, it quells the pathogen's propagation, sieging its lethal ambitions. Synonyms: 3'-O-Allyl-dA. Grade: ≥97% by HPLC. Molecular formula: C13H17N5O3. Mole weight: 291.31. | |
| 3'-O-Allyl-2'-deoxycytidine | 3'-O-Allyl-2'-deoxycytidine is a modified nucleoside where an allyl group is attached to the 3' position of the 2'-deoxyribose sugar in a cytidine molecule. The modification of the 3' hydroxyl group with an allyl group alters the compound's chemical reactivity and may affect its interaction with enzymes or other molecular targets. Such modifications can enhance the stability of the nucleoside in DNA sequences, potentially improving its pharmacokinetic properties for applications in nucleic acid-based therapies, such as gene therapy, or for use in oligonucleotide synthesis. The allyl group could also serve as a handle for further chemical modifications or conjugation to other biomolecules. Synonyms: 2'-Deoxy-3'-O-2-propen-1-ylcytidine; 3'-O-Allyl dC; 3-O-Allyl-2-Deoxycytidine; 1-((2R,4S,5R)-4-(Allyloxy)-5-(hydroxymethyl)tetrahydrofuran-2-yl)-4-aminopyrimidin-2(1H)-one. Grade: ≥98%. CAS No. 925915-24-8. Molecular formula: C12H17N3O4. Mole weight: 267.28. | |
| 3'-O-Allyl-2'-deoxyguanosine | 3'-O-Allyl-2'-deoxyguanosine, a nucleoside analogue extensively employed in the biomedical sector, serves as a fundamental tool to examine the suppression of viral replication. Exceptionally capable of curbing the propagation of human immunodeficiency virus (HIV), this product offers exceptional prospects for antiviral therapy. Expanding beyond antiviral applications, its powerful apoptotic effects on cancer cells make it a promising contender in the realm of cancer therapies. Synonyms: 3'-O-Allyl-dG; 2-amino-9-[(2R,4S,5R)-5-(hydroxymethyl)-4-prop-2-enoxyoxolan-2-yl]-1H-purin-6-one. Grade: ≥97% by HPLC. Molecular formula: C13H17N5O4. Mole weight: 307.31. | |
| 3'-O-Allyl-2'-deoxyuridine | 3'-O-Allyl-2'-deoxyuridine, a nucleoside analogue, harbors significant potential in exhibiting antiviral activity against the herpes simplex virus, which has been studied extensively for its application in treating herpes simplex encephalitis - a virulent infection of the brain caused by the herpes simplex virus, with a potential to unleash a life-threatening threat. Synonyms: 3'-O-Allyl-dU. Grade: ≥97% by HPLC. Molecular formula: C12H16N2O5. Mole weight: 268.27. | |
| 3'-(O-Allyl)-adenosine | 3'-(O-Allyl)-adenosine is a formidable nucleoside analog used in the research of malignant neoplasms and insidious viral invasions, adroitly navigating the intricate path paved by the ever-enticing adenosine receptors. Grade: ≥ 98% by HPLC. Molecular formula: C13H17N5O4. Mole weight: 307.31. | |
| 3'-O-Allyladenosine | 3'-O-Allyladenosine, a vital compound in the field of biomedicine, serves as a fundamental element for investigating adenosine receptors. These receptors, implicated in a multitude of ailments encompassing cardiovascular disorders, immunological responses, and neurodegenerative afflictions, hold great importance. This particular product is frequently employed to delve into the potential therapeutic applications of adenosine receptor modulation, specifically targeting conditions like ischemic heart disease, asthma, and malignancies. Synonyms: 3'-O-Allyl-D-adenosine; 3'-(O-allyl) Adenosine; 3'-O-allyl Adenosine; (2R,3R,4S,5R)-4-(allyloxy)-2-(6-amino-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3-ol; 3'-O-2-Propen-1-yladenosine. Grade: 98%. CAS No. 400820-99-7. Molecular formula: C13H17N5O4. Mole weight: 307.31. | |
| 3-O-Allyl-β-D-glucopyranose | 3-O-Allyl-β-D-glucopyranose. Synonyms: 3-O-2-Propen-1-yl-beta-d-glucopyranose; 3-O-2-Propen-1-yl-β-D-glucopyranose. CAS No. 77388-91-1. Molecular formula: C9H16O6. Mole weight: 220.22. | |
| 3'-(O-Allyl)-cytidine | 3'-(O-Allyl)-cytidine is a treasured compound, unveiling its prowess in the realm of antiviral drug research and development. Grade: ≥ 98% by HPLC. Molecular formula: C12H17N3O5. Mole weight: 283.28. | |
| 3'-O-Allylcytidine | 3'-O-Allylcytidine, a cutting-edge biomedical innovation, stands as a pivotal resource in combating a wide range of diseases. It showcases an exquisite modification of cytidine, unveiling extraordinary potential in the selective eradication of cancerous cells and hindering their malignant proliferation. Furthermore, this compound's remarkable antiviral attributes have garnered significant attention, empowering its utilization against specific strains of viral infections. Synonyms: 3'-O-Allyl-D-cytidine; 3'-(O-allyl) Cytidine; 1-((2R,3R,4S,5R)-4-(allyloxy)-3-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-4-aminopyrimidin-2(1H)-one. Grade: 98%. Molecular formula: C12H17N3O5. Mole weight: 283.28. | |
| 3'-(O-Allyl)-guanosine | 3'-(O-Allyl)-guanosine is a vital biomedical entity, has garnered significant attention for its profound therapeutic potential in addressing a wide array of afflictions encompassing viral infections, malignancies, and inflammatory maladies. Distinguished for its commendable capacity to impede viral replication, this remarkable compound emerging as a formidable antiviral compound. Moreover, its prowess extends to the suppression of tumorigenesis and the orchestration of apoptosis, rendering it a promising anticancer combatant. Furthermore, its innate ability to intricately modulate the immune response augments its therapeutic significance in attenuating deleterious inflammatory cascades. Unquestionably, this mesmerizing compound embodies an indispensable cornerstone in the sphere of biomedical exploration and pharmaceutical innovation. Grade: ≥ 98% by HPLC. Molecular formula: C13H17N5O5. Mole weight: 323.3. | |
| 3'-O-Allylguanosine | 3'-O-Allylguanosine, a widely used biomedicine product in research, presents itself as a paramount avenue to explore the antiviral properties exhibited by guanosine derivatives. Its prominent role extends to serving as a pivotal reference compound, wherein its efficacy in combating viral infections, namely HIV, hepatitis, and respiratory viruses, can be meticulously evaluated. Synonyms: 3'-(O-allyl) Guanosine; 3'-O-Allyl-D-guanosine; 9-((2R,3R,4S,5R)-4-(allyloxy)-3-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-amino-1,9-dihydro-6H-purin-6-one. Grade: 98%. Molecular formula: C13H17N5O5. Mole weight: 323.30. | |
| 3'-O-Allylthymidine | 3'-O-Allylthymidine, a potent nucleoside analog, possesses impactful antiviral activity against human immunodeficiency virus (HIV) and herpes viruses. Besides being a valuable substrate for biochemical assays that study reverse transcriptase, it also demonstrates promising potential for anticancer therapy. Synonyms: 3'-O-Allyl-dT; Thymidine, 3'-O-2-propen-1-yl-. Grade: ≥97% by HPLC. CAS No. 211191-57-0. Molecular formula: C13H18N2O5. Mole weight: 282.29. | |
| 3'-(O-Allyl)-uridine | 3'-(O-Allyl)-uridine is a remarkable compound, exhibiting immense potential in combatting an array of viral infections such as hepatitis C and HIV. By diligently stifling viral replication while effectively stimulating the body's formidable immune response, it distinguishes itself as a formidable adversary against these relentless pathogens. This invaluable resource burgeons opportunities in the realm of research and development, fostering the research and development of novel antiviral drugs and vaccines, ultimately ensuring enhanced efficacies in overthrowing these notorious afflictions. Grade: ≥ 98% by HPLC. Molecular formula: C12H16N2O6. Mole weight: 284.27. | |
| 3'-O-Allyluridine | 3'-O-Allyluridine, a vital compound extensively employed in the biomedical sector, plays a pivotal role in combating diverse ailments. Brimming with extraordinary antiviral and anticancer attributes, this remarkable entity boasts immense worth in the realm of antiviral medications and chemotherapeutic agents. With its profound ability to specifically target and impede the replication of both viruses and malignant cells, this compound unfurls a vast array of prospects for potential therapeutic interventions against viral infections and neoplastic disorders. Synonyms: 3'-(O-allyl) Uridine; 3'-O-Allyl-D-uridine; 1-((2R,3R,4S,5R)-4-(allyloxy)-3-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)pyrimidine-2,4(1H,3H)-dione. Grade: 95%. Molecular formula: C12H16N2O6. Mole weight: 284.27. | |
| 3-O-α-L-Fucopyranosyl-D-galactose | 3-O-α-L-Fucopyranosyl-D-galactose. Synonyms: 3-O-(6-Deoxy-α-L-galactopyranosyl)-D-galactose. CAS No. 24667-49-0. Molecular formula: C12H22O10. Mole weight: 326.30. | |
| 3-O-α-L-Fucopyranosyl-D-glucose | 3-O-α-L-Fucopyranosyl-D-glucose. Synonyms: 3-O-(6-Deoxy-α-L-galactopyranosyl)-D-glucose. CAS No. 56822-52-7. Molecular formula: C12H22O10. Mole weight: 326.30. | |
| 3'-O-Amino-2'-deoxyadenosine | 3'-O-Amino-2'-deoxyadenosine is an indispensable compound extensively employed in the biomedical sector, serving as a pivotal constituent in the fabrication of antiviral remedies and nucleotide analogs. Renowned for its exclusive structural attributes, this compound assumes paramount significance in research of diverse viral ailments such as hepatitis B and HIV. CAS No. 132471-87-5. Molecular formula: C10H14N6O3. Mole weight: 266.26. | |
| 3'-O-Amino-2'-deoxyadenosine 5'-triphosphate | 3'-O-Amino-2'-deoxyadenosine 5'-triphosphate is a crucial nucleotide derivative widely utilized in the field of biomedicine. It plays a vital role in various biochemical assays and experiments, particularly in the study of DNA replication, repair, and modification processes. Due to its unique molecular structure, it is frequently employed in research related to drug development, DNA sequencing, and targeted therapies for diseases such as cancer and genetic disorders. Synonyms: 3'-ONH2-dATP Sodium Salt; (((2R,3S,5R)-5-(6-amino-9H-purin-9-yl)-3-(aminooxy)tetrahydrofuran-2-yl)methyl)triphosphoric acid. Grade: 98%. CAS No. 1220515-87-6. Molecular formula: C10H17N6O12P3. Mole weight: 506.20. | |
| 3'-O-Amino-2'-deoxycytidine | 3'-O-Amino-2'-deoxycytidine is a vital compound widely used in the biomedical industry playing a significant role in studying diseases related to the DNA replication and research and development process. Specifically, it is utilized in the development of novel antiviral drugs as well as in research focused on understanding and research of genetic disorders. Synonyms: 3'-O-Amino-dC. Grade: ≥98% by HPLC. CAS No. 103251-39-4. Molecular formula: C9H14N4O4. Mole weight: 242.23. | |
| 3'-O-Amino-2'-deoxycytidine 5'-triphosphate | 3'-O-Amino-2'-deoxycytidine 5'-triphosphate, an essential molecule in the realm of DNA investigation and biomedical studies, assumes the position of a paramount reagent. Within enzymatic polymerization processes, this valuable substrate readily partakes, thus facilitating DNA molecule synthesis. By engaging with the mechanisms underpinning DNA replication and repair, this product assumes an indispensable role. Moreover, its utilization extends to probing diseases elucidated by DNA mutations. Synonyms: 3'-O-Amino-2'-deoxycytidine 5'-triphosphate; SCHEMBL1333569; A902410; 3'-O-amino-2'-deoxy-Cytidine 5'-(tetrahydrogen triphosphate); (((2R,3S,5R)-5-(4-amino-2-oxopyrimidin-1(2H)-yl)-3-(aminooxy)tetrahydrofuran-2-yl)methyl)triphosphoric acid. CAS No. 1220515-75-2. Molecular formula: C9H17N4O13P3. Mole weight: 482.17. | |
| 3'-O-Aminothymidine | 3'-O-Aminothymidine, a nucleoside analogue, is efficacious in treating different viral infections such as HIV and hepatitis B by restricting viral DNA synthesis and hindering further viral multiplication. Remarkably, it exhibits promising therapeutic effects against certain cancer types, notably leukemia and lymphoma. Its antiviral and antiproliferative properties make it an excellent candidate for drug development and treatment. Synonyms: 3'-O-Amino-dT; 3'-O-Amino-2'-deoxythymidine; 1-(3-O-Amino-2-deoxypentofuranosyl)-4-hydroxy-5-methylpyrimidin-2(1H)-one; 1-((2R,4S,5R)-4-(Aminooxy)-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione. Grade: ≥98% by HPLC. CAS No. 103251-38-3. Molecular formula: C10H15N3O5. Mole weight: 257.24. | |
| 3'-O-Aminothymidine-5'-triphosphate | 3'-O-Aminothymidine-5'-triphosphate is a remarkably significant constituent within the realm of compound, epitomizing a substrate of paramount importance. Consequently, its distinctive structural attributes engender its exploitation in DNA replication and research and development. Notably, this invaluable compound assumes a pivotal function in diverse investigations pertaining to the development of antiviral therapeutics and the molecular diagnosis of afflictions such as neoplastic disorders and viral infections. CAS No. 1159990-37-0. | |
| 3'-O-Azidomethyl 2'-deoxyadenosine 5'-O-triphosphate sodium salt | 3'-O-Azidomethyl 2'-deoxyadenosine 5'-O-triphosphate sodium salt is a vital tool in compound used for DNA labeling, research and development is and modification. It acts as a specific substrate for DNA polymerases in amplification reactions aiding in the study of drug-resistant mutations and genetic diseases. This sodium salt provides high efficiency and accuracy in site-specific incorporation during enzymatic DNA research and development or nucleic acid labeling, making it an indispensable component in various biomedical research applications. Synonyms: 3'-O-Azidomethyl-dATP.Na. Molecular formula: C11H17N8O12P3. Mole weight: 546.22. | |
| 3'-O-Azidomethyl-dATP | 3'-O-Azidomethyl-dATP is a crucial reagent in compound utilized for efficient DNA labeling and analysis serving as a precursor in diverse applications such as DNA sequencing, nucleic acid labeling is and Click chemistry. The azide group allows for subsequent attachment of various functional moieties, enabling site-specific modification and investigation of DNA-protein interactions or DNA structure-function relationships. Synonyms: 3'-O-Azidomethyl-2'-deoxyadenosine-5'-triphosphate, Sodium salt. Grade: ≥ 95% by HPLC. Molecular formula: C11H17N8O12P3 (free acid). Mole weight: 546.22 (free acid). | |
| 3'-O-Azidomethyl-dCTP | 3'-O-Azidomethyl-dCTP is a nucleotide analog, through its enzymatic incorporation into DNA strands, catalyzing eminent modifications and labeling. In the realm of DNA research and development and amplification, this exalted entity assumes a pivotal role, unraveling the mysteries intertwined within DNA-protein interactions, gene expression is and the profound complexities of DNA sequencing technologies. Synonyms: 3'-O-Azidomethyl-2'-deoxycytidine-5'-triphosphate, Sodium salt. Grade: ≥ 95% by HPLC. Molecular formula: C10H17N6O13P3 (free acid). Mole weight: 520.20 (free acid). | |
| 3'-O-Azidomethyl-Deoxyguanosine Triphosphate (dGTP) | 3'-O-Azidomethyl-Deoxyguanosine Triphosphate (dGTP) is a crucial tool in biomedical research for the synthesis of modified DNA. It serves as a substrate for DNA polymerases is allowing the incorporation of azide-modified deoxyguanosine into DNA strands. This modified nucleotide is useful for various applications, including labeling, click chemistry and cross-linking studies. Additionally, it finds application in drug development and the study of DNA-protein interactions in diseases like cancer. Grade: > 95%. Molecular formula: C11H17N8O13P3. Mole weight: 562.23. | |
| 3'-O-Azidomethyl-dTTP | 3'-O-Azidomethyl-dTTP is a chemical compound highly prevalent in the biomedical sector assuming a paramount function by means of its application in the labeling and modification of nucleic acid molecules. Profoundly employed within diverse research domains, such as DNA sequencing, nucleic acid amplification is and the exploration of DNA-protein interactions, this compound unveils an unprecedented avenue to unravel and grasp the intricate molecular mechanisms underlying a myriad of afflictions. Synonyms: 3'-O-Azidomethyl-2'-deoxythymidine-5'-triphosphate, Sodium salt. Grade: ≥ 95% by HPLC. Molecular formula: C11H18N5O14P3 (free acid). Mole weight: 537.21 (free acid). | |
| 3-O-(b-D-Galactopyranosyl)-D-arabinose | 3-O-(b-D-Galactopyranosyl)-D-arabinose, known for its significant role in the biomedicine industry, stands as a pivotal compound with immense potential as a therapeutic agent against a multitude of ailments encompassing cancer and viral infections. By virtue of its remarkable structure and distinctive properties, it emerges as an indispensable constituent within pharmaceutical formulations. Synonyms: 3-O-β-D-Galactopyranosyl-D-arabinose; Arabinose, 3-O-β-D-galactopyranosyl-, D-; Galarose. CAS No. 6057-48-3. Molecular formula: C11H20O10. Mole weight: 312.27. | |
| 3-O-(b-D-Galactopyranosyl)-D-galactopyranose | 3-O-(b-D-Galactopyranosyl)-D-galactopyranose is a valuable compound utilized in the research and development of drugs aimed at studying various diseases, including cancer, diabetes and inflammation. Additionally, this compound has potential applications in the research of regenerative medicine due to its ability to promote tissue repair and regeneration. Synonyms: b1-3Galactobiose. Molecular formula: C12H22O11. Mole weight: 342.30. | |
| 3-O-(b-D-Galactopyranosyl)-D-glucopyranose | 3-O-(b-D-Galactopyranosyl)-D-glucopyranose is an indispensable carbohydrate compound in the biomedical industry, facilitating a comprehensive elucidation of sugar metabolism whilst diligently exploring therapeutic glycosylation pathways. Synonyms: 3-O-beta-D-Galactopyranosyl-D-glucopyranose; 3-O-(b-D-Galactopyranosyl)-D-glucopyranose; Gal(b1-3)Glc; beta-D-Galp-(1->3)-D-Glcp; beta-D-galacto-hexopyranosyl-(1->3)-D-gluco-hexopyranose. CAS No. 28447-38-3. Molecular formula: C12H22O11. Mole weight: 342.30. | |
| 3-O-(b-D-Galactopyranosyl)-D-mannopyranose | 3-O-(b-D-Galactopyranosyl)-D-mannopyranose is an essential element utilized in development of medicinal remedies. Its research involvement extends to diverse ailments, especially those linked to irregular glycosylation patterns. Molecular formula: C12H22O11. Mole weight: 342.30. | |
| 3-O-b-D-Galactosylsucrose | 3-O-b-D-Galactosylsucrose. CAS No. 686717-73-7. Molecular formula: C18H32O16. Mole weight: 504.4. | |
| 3-O-(b-D-Glucopyranosyl)-L-DOPA | 3-O-(b-D-Glucopyranosyl)-L-DOPA is a bioactive compound, holding immense potential in research of Parkinson's disease. As a derivative of the precursor L-DOPA, it intricately intertwines with the metabolic process, enhancing its bioavailability. Molecular formula: C15H21NO9. Mole weight: 359.33. | |
| 3'-O-(b-D-Glucopyranosyl)-L-DOPA | 3'-O-(b-D-Glucopyranosyl)-L-DOPA, a well-known compound within the biomedical industry, serves a pivotal function in the treatment of Parkinson's disease by acting as a precursor for dopamine synthesis in the brain. By effectively heightening dopamine levels, it exhibits the capacity to enhance motor symptoms and overall quality of life for patients. Synonyms: 3-(beta-D-Glucopyranosyloxy)-L-tyrosine; 3-(β-D-Glucopyranosyloxy)-L-tyrosine; Alanine, 3-[3-(β-D-glucopyranosyloxy)-4-hydroxyphenyl]-, L-; 3-O-β-D-Glucopyranosyl L-DOPA. CAS No. 2275-95-8. Molecular formula: C15H21NO9. Mole weight: 359.33. | |
| 3-O-(b-D-Mannopyranosyl)-D-mannose | 3-O-(b-D-Mannopyranosyl)-D-mannose, a pivotal biomolecule in medical science, exhibits an intricate architecture. It finds extensive application in crafting curative interventions for a diverse range of ailments like diabetes and metabolic disorders. Its profound chemical structure and exceptional attributes render it an indispensable substance in the realm of pharmaceutical exploration and advancement. Synonyms: b-D-Man-[1-3]D-man; 3b-Mannobiose; D-Mannose, 3-O-β-D-mannopyranosyl-; 3-O-β-D-Mannopyranosyl-D-mannose. CAS No. 50692-75-6. Molecular formula: C12H22O11. Mole weight: 342.30. | |
| 3'-O-Benzoyl-2'-deoxyuridine | 3'-O-Benzoyl-2'-deoxyuridine, an indispensible biomedical compound, finds application in the realm of antiviral research and pharmaceutical innovation. Its paramount function encompasses curtailing viral replication, primarily targeting cytomegalovirus and herpes simplex virus. Endowed with a distinctive composition and intricate mechanism, this compound emerges as a promising contender for impeding viral afflictions and propelling advancements in the sphere of antiviral therapies. Synonyms: 3'-O-Benzoyl-2'-deoxy-D-uridine. Grade: 98%. CAS No. 53213-02-8. Molecular formula: C16H16N2O6. Mole weight: 332.31. | |
| 3-O-Benzyl-1,2:5,6-di-O-cyclohexylidene-a-D-glucofuranose | 3-O-Benzyl-1,2:5,6-di-O-cyclohexylidene-a-D-glucofuranose is a truly remarkable and indispensable compound serving as a pivotal constituent for the creation of groundbreaking pharmaceuticals and carbohydrate-based medicinal wonders. This prodigious entity showcases its distinctive architecture and unrivaled reactivity. Synonyms: 3-O-Benzyl-1,2,5,6-di-O-cyclohexylidene-alpha-D-glucofuranose; 1,2:5,6-Di-O-cyclohexylidene-3-O-(phenylmethyl)-alpha-D-glucofuranose. CAS No. 13322-88-8. Molecular formula: C25H34O6. Mole weight: 430.53. | |
| 3-O-Benzyl-1,2:5,6-di-O-isopropylidene-a-D-allofuranose | 3-O-Benzyl-1,2:5,6-di-O-isopropylidene-a-D-allofuranose is an eminent compound extensively employed in the biomedical sector for a myriad of purposes, presenting itself as a momentous entity in drug discovery endeavors. This compound encapsulates promising prospects in the realms of cancer, diabetes is and inflammation research. Synonyms: 3-O-Benzyl-1,2:5,6-bis-O-isopropylidene-alpha-D-galactofuranose; (3aR,5R,6R,6aR)-6-(benzyloxy)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole. CAS No. 22331-21-1. Molecular formula: C19H26O6. Mole weight: 350.41. | |
| 3-O-Benzyl-1,2:5,6-di-O-isopropylidene-a-D-glucofuranose | 3-O-Benzyl-1,2:5,6-di-O-isopropylidene-α-D-glucofuranose, a profound constituent within the realm of biomedical science, renders it indispensable in the synthesis of an array of pharmacological agents studying multifarious maladies including carcinogenesis, diabetes mellitus, and viral pathogenesis. Synonyms: 3-O-Benzyl-1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranose; 1,2:5,6-Bis-O-(1-methylethylidene)-3-O-(phenylmethyl)-alpha-D-glucofuranose. CAS No. 18685-18-2. Molecular formula: C19H26O6. Mole weight: 350.41. | |
| 3-O-Benzyl-1,2-O-isopropylidene-6-O-pivaloyl-a-D-glucofuranose | 3-O-Benzyl-1,2-O-isopropylidene-6-O-pivaloyl-a-D-glucofuranose is a paramount entity in the biomedical realm, used for synthesizing diverse pharmaceuticals aimed at maladies entwined with glucose metabolism and carbohydrate chemistry. Synonyms: (R)-2-((3AR,5R,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)-2-hydroxyethyl pivalate; 321380-09-0. CAS No. 321380-09-0. Molecular formula: C21H30O7. Mole weight: 394.46. | |
Our database is helping our users find suppliers everyday.
