Alfa Chemistry. - Products
Alfa Chemistry is an ISO 9001:2015 Certified Supplier of various building blocks, reagents, catalysts, nanomaterials, reference materials, and research chemicals. In-stock products can be shipped quickly.
| Product | Description | |
|---|---|---|
| Boc-Cys-OH (cryst) | Building block for preparation of Boc-Cys derivatives. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Cys-OH (cryst), N-α-t.-Boc-L-cysteine. CAS No. 20887-95-0. Mole weight: 221.27. Catalog: ACM20887950. |  |
| Boc-Cys(Trt)-OH | Building block for introduction of N-terminal cysteinyl residues in Boc SPPS Fmoc SPPS of Cysteine-Containing Peptides. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Cys(Trt)-OH, N-α-t.-Boc-S-trityl-L-cysteine. CAS No. 21947-98-8. Molecular formula: C27H29NO4S. Mole weight: 463.59. Catalog: ACM21947988. | |
| Boc-D-Ala-OH | Standard building block for introduction of D-alanine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Ala-OH, N-α-t.-Boc-D-alanine. CAS No. 7764-95-6. Mole weight: 189.21. Catalog: ACM7764956. | |
| Boc-D-arg-oh · hcl · h2o | Heterocyclic Organic Compound. Alternative Names: Boc-D-Arg-OH. HCl;Boc-D-Arg-OH H2O HCl;N-alpha-tert-Butyloxycarbonyl-D-arginine1-hydrate hydrochloride. CAS No. 113712-06-4. Molecular formula: C11H22N4O4·HCl·H2O. Mole weight: 328.8. Purity: 0.96. IUPACName: (2R)-5-(diaminomethylideneamino)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid;hydrate;hydrochloride. Canonical SMILES: CC(C)(C)OC(=O)NC(CCCN=C(N)N)C(=O)O. Cl. ECNumber: 601-276-0. Catalog: ACM113712064. | |
| Boc-D-Arg(Tos)-OH | Building block for introduction of D-arginine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Arg(Tos)-OH, N-α-t.-Boc-N G-tosyl-D-arginine. CAS No. 61315-61-5. Mole weight: 428.5. Catalog: ACM61315615. | |
| Boc-D-Asn-OH | Standard building block for introduction of D-asparagine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Asn-OH, N-α-t.-Boc-D-asparagine. CAS No. 75647-01-7. Mole weight: 232.23. Catalog: ACM75647017. | |
| Boc-D-aspartic acid 4-cyslohexyl ester | Heterocyclic Organic Compound. CAS No. 112898-18-7. Molecular formula: C15H25NO6. Mole weight: 315.36. Catalog: ACM112898187. | |
| Boc-D-Asp(OBzl)-OH | Standard building block for introduction of D-aspartic acid amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Asp(OBzl)-OH, N-α-t.-Boc-D-aspartic acid β-benzyl ester. CAS No. 51186-58-4. Mole weight: 323.34. Catalog: ACM51186584. | |
| Boc-D-Cys(Acm)-OH | Standard building block for introduction of D-cysteine amino-acid residues by Boc SPPS. Fmoc SPPS of Cysteine-Containing Peptides. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Cys(Acm)-OH, N-α-t.-Boc-S-acetamidomethyl-D-cysteine. CAS No. 138775-00-5. Mole weight: 292.35. Catalog: ACM138775005. | |
| Boc-D-Cys(Trt)-OH | Building block for introduction of N-terminal D-cysteine amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Cys(Trt)-OH, N-α-t.-Boc-S-trityl-D-cysteine. CAS No. 87494-13-1. Mole weight: 463.59. Catalog: ACM87494131. | |
| Boc-D-Glu-OBzl | Standard building block for introduction of D-γ-glutamic acid amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Glu-OBzl, N-α-t.-Boc-D-glutamic acid α-benzyl ester. CAS No. 34404-30-3. Mole weight: 337.37. Catalog: ACM34404303. | |
| Boc-D-Glu(OBzl)-OH | Standard building block for introduction of D-glutamic acid amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Glu(OBzl)-OH, N-α-t.-Boc-D-glutamic acid γ-benzyl ester. CAS No. 35793-73-8. Mole weight: 337.37. Catalog: ACM35793738. | |
| Boc-D-His-OH | Standard building block for introduction of D-histidine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-His-OH, N-α-t.-Boc-D-histidine. CAS No. 50654-94-9. Mole weight: 255.27. Catalog: ACM50654949. | |
| Boc-D-lys(fmoc)-oh | Heterocyclic Organic Compound. CAS No. 115186-31-7. Molecular formula: C26H32N2O6. Mole weight: 468.54. Catalog: ACM115186317. | |
| Boc-D-Met-OH | Standard building block for introduction of D-methionine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Met-OH, N-α-t.-Boc-D-methionine. CAS No. 5241-66-7. Mole weight: 249.33. Catalog: ACM5241667. | |
| Boc-D-Phe-OH | Standard building block for introduction of D-phenylalanine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Phe-OH, N-α-t.-Boc-D-phenylalanine. CAS No. 18942-49-9. Mole weight: 265.3. Catalog: ACM18942499. | |
| Boc-D-Pro-OH | Standard building block for introduction of D-proline amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Pro-OH, N-α-t.-Boc-D-proline. CAS No. 37784-17-1. Mole weight: 215.25. Catalog: ACM37784171. | |
| Boc-D-Ser(Bzl)-OH | Standard building block for introduction of D-serine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Ser(Bzl)-OH, N-α-t.-Boc-O-benzyl-D-serine. CAS No. 47173-80-8. Mole weight: 295.33. Catalog: ACM47173808. | |
| Boc-D-Ser-OH | Standard building block for introduction of D-serine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Ser-OH, N-α-t.-Boc-D-serine. CAS No. 6368-20-3. Mole weight: 205.21. Catalog: ACM6368203. | |
| Boc-D-Thr(Bzl)-OH | Standard building block for introduction of D-threonine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Thr(Bzl)-OH, N-α-t.-Boc-O-benzyl-D-threonine / (2R,3S). CAS No. 69355-99-3. Mole weight: 309.36. Catalog: ACM69355993. | |
| Boc-D-Trp-OH | Standard building block for introduction of D-tryptophan amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Trp-OH, N-α-t.-Boc-D-tryptophan. CAS No. 5241-64-5. Mole weight: 304.34. Catalog: ACM5241645. | |
| Boc-D-Tyr(Bzl)-OH | Standard building block for introduction of D-tyrosine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Tyr(Bzl)-OH, N-α-t.-Boc-O-benzyl-D-tyrosine. CAS No. 63769-58-4. Mole weight: 371.43. Catalog: ACM63769584. | |
| Boc-D-Tyr-OH | Standard building block for introduction of D-tyrosine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Tyr-OH, N-α-t.-Boc-D-tyrosine. CAS No. 70642-86-3. Mole weight: 281.3. Catalog: ACM70642863. | |
| Boc-D-Val-OH | Standard building block for introduction of D-valine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-D-Val-OH, N-α-t.-Boc-D-valine. CAS No. 22838-58-0. Mole weight: 217.26. Catalog: ACM22838580. | |
| Boc-ε-Ahx-OH | Standard building block for introduction of aminohexanoic acid amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-ε-Ahx-OH, N-ε -t.-Boc-ε -aminocaproic acid,t.-Boc-6-aminohexanoic acid. CAS No. 6404-29-1. Molecular formula: C11H21NO4. Mole weight: 231.29. Catalog: ACM6404291. | |
| Boc-γ-Abu-OH | Standard building block for introduction of γ-aminobutyric acid amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-γ-Abu-OH, t.-Boc-4-aminobutanoic acid,t.-Boc-GABA. CAS No. 57294-38-9. Mole weight: 203.24. Catalog: ACM57294389. | |
| Boc-gln-ala-arg-7-amino-4-methylcoumarin | Heterocyclic Organic Compound. CAS No. 113866-20-9. Molecular formula: C29H42N8O8. Mole weight: 630.69. Catalog: ACM113866209. | |
| Boc-Gln-OH | Standard building block for introduction of glutamine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Gln-OH, N-α-t.-Boc-L-glutamine. CAS No. 13726-85-7. Mole weight: 246.26. Catalog: ACM13726857. | |
| Boc-Gln(Trt)-OH | A trityl-protected derivative which increases the solubility of glutamine during the coupling step in SPPS. Its use gives higher yields and lower by-product formation. During the following coupling cycles the temporary side-chain protection is removed. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Gln(Trt)-OH, N-α-t.-Boc-γ-trityl-L-glutamine. CAS No. 132388-69-3. Mole weight: 488.57. Catalog: ACM132388693. | |
| Boc-Glu-OBzl | Useful derivative for the synthesis of γ-glutamyl peptides. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-L-glutamic acid 1-benzyl ester. CAS No. 30924-93-7. Mole weight: 337.37. Canonical SMILES: CC (C) (C)OC (=O)N[C@@H] (CCC (O)=O)C (=O)OCc1ccccc1. Catalog: ACM30924937. | |
| Boc-glu(obzl)-ala-arg-mca | Heterocyclic Organic Compound. Alternative Names: T-BUTYLOXYCARBONYL-[(2S)-2-AMINO-4-(BENZYLOXYCARBONYL)BUTANOYL]-L-ALANYL-L-ARGININE 4-METHYLCOUMARYL-7-AMIDE;BOC-GLU(OBZL)-ALA-ARG-MCA. CAS No. 113866-16-3. Molecular formula: C36H47N7O9. Mole weight: 721.8. Catalog: ACM113866163. | |
| Boc-Glu(OBzl)-OH | Building block for introduction of glutamic acid amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Glu(OBzl)-OH, N-α-t.-Boc-L-glutamic acid γ-benzyl ester. CAS No. 13574-13-5. Mole weight: 337.37. Catalog: ACM13574135-1. | |
| Boc-Glu-OH | Derivative of synthesis of side-chain modified glutamic acid derivatives. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Glu-OH, N-α-t.-Boc-L-glutamic acid. CAS No. 2419-94-5. Mole weight: 247.25. Catalog: ACM2419945. | |
| Boc-Glu-OtBu | Derivative of synthesis of side-chain modified glutamic acid derivatives. Uses: Boc-glu-otbu is an n-terminal protected amino acid used in solid-phase peptide synthesis (spps) to make unique peptides containing glutamate tert-butyl ester residues. Group: Amino acids. Alternative Names: Boc-L-glutamic acid 1-tert-butyl ester. CAS No. 24277-39-2. Mole weight: 303.35. Canonical SMILES: CC (C) (C)OC (=O)N[C@@H] (CCC (O)=O)C (=O)OC (C) (C)C. Catalog: ACM24277392. | |
| Boc-Glu(OtBu)-OH | Building block of introduction of N-terminal glutamic acid amino-acid residues by Fmoc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Glu(OtBu)-OH, N-α-t.-Boc-L-glutamic acid γ-t.-butyl ester. CAS No. 13726-84-6. Mole weight: 303.35. Catalog: ACM13726846. | |
| Boc-Gly-OH | Standard building block for introduction of glycine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Gly-OH, N-α-t.-Boc-glycine. CAS No. 4530-20-5. Molecular formula: C7H13NO4. Mole weight: 175.18. Catalog: ACM4530205. | |
| Boc-grr-amc | Heterocyclic Organic Compound. Alternative Names: T-BUTYLOXYCARBONYLGLYCYL-L-ARGINYL-L-ARGININE 4-METHYLCOUMARYL-7-AMIDE;BOC-GRR-AMC;BOC-GLY-ARG-ARG-MCA;BOC-GLY-ARG-ARG-AMC;TERT-BUTYLOXYCARBONYL-GLYCYL-L-ARGINYL-L-ARGININE 4-METHYLCOUMARYL-7-AMIDE. CAS No. 113866-14-1. Molecular formula: C29H44N10O7. Mole weight: 644.72. Catalog: ACM113866141. | |
| Boc-His(Boc)-OH. DCHA | A protected histidine derivative for only the critical coupling step in Boc SPPS. After coupling the two Boc-groups are cleaved simultaneously by TFA. Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-His(Boc)-OH. DCHA, N-α-N-im-di-t.-Boc-L-histidine dicyclohexylammonium salt. CAS No. 31687-58-8. Mole weight: 355.39. Catalog: ACM31687588. | |
| Boc-His-OH | Building block for introduction of histidine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-His-OH, N-α-t.-Boc-L-histidine. CAS No. 17791-52-5. Mole weight: 255.27. Catalog: ACM17791525. | |
| Boc-His(Trt)-OH | A protected histidine derivative for only the critical coupling step in Boc SPPS. After coupling the Boc- and Trt-groups are cleaved simultaneously by TFA. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-His(Trt)-OH, N-α-t.-Boc-N-im-trityl-L-histidine. CAS No. 32926-43-5. Mole weight: 497.58. Catalog: ACM32926435. | |
| Bocidelpar | Bocidelpar, also known as ASP0367 or MA-0211, is a peroxisome proliferator-activated receptor (PPAR) delta agonist. Group: Agonists. Alternative Names: Bocidelpar; ASP0367; SP-0367 ; SP 0367; MA-0211; MA 0211; MA0211. CAS No. 2095128-20-2. Molecular formula: C25H27F3N2O3. Mole weight: 460.5. Appearance: Solid powder. Purity: >98%. IUPACName: (3R)-3-methyl-6-[2-({5-methyl-2-[4-(trifluoromethyl)phenyl]-1H-imidazol-1-yl}methyl)phenoxy]hexanoic acid. Canonical SMILES: O=C (O)C[C@H] (C)CCCOC1=CC=CC=C1CN2C (C)=CN=C2C3=CC=C (C (F) (F)F)C=C3. Catalog: ACM2095128202. | |
| Boc-L-2-amino-5-phenylpentanoic acid dicyclohexylamine salt | Heterocyclic Organic Compound. Alternative Names: Boc-L-2-Amino-5-phenyl-pentanoic acid·DCHA;Benzenepentanoic acid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-, (S)-, compd. with N-cyclohexylcyclohexanamine (1:1). CAS No. 113756-89-1. Molecular formula: C16H23NO4.C12H23N. Mole weight: 474.68. Catalog: ACM113756891. | |
| Boc-L-Ile-CHN2 | Heterocyclic Organic Compound. Alternative Names: BOC-L-ILE-CHN2; N-ALPHA-T-BUTYLOXYCARBONYL-L-ISOLEUCINYL-DIAZOMETHANE; (3S,4S)-N-TERTIARY-BUTOXYCARBONYLISOLEUCINYL DIAZOMETHANE. CAS No. 114645-19-1. Molecular formula: C12H21N3O3. Mole weight: 255.32. Purity: 0.96. IUPACName: [(3S,4S)-N-tert-Butoxycarbonyl-L-isoleucyl]diazomethane. Catalog: ACM114645191. | |
| Boc-L-thyroxine | Boc-T4 is a synthetic prodrug of thyroxine, a hormone produced by the thyroid gland that plays a crucial role in regulating metabolism and other physiological processes. Boc-T4 is designed to be a prodrug that can be activated by enzymes in the body to release thyroxine slowly over a prolonged period. This approach can reduce the dosage frequency and provide a more sustained release of the hormone. Uses: Boc-t4 has potential applications in various fields of research and industry, including drug development, biomedical research, and agriculture. the compound can be used as a prodrug for thyroxine, providing a more sustained release of the hormone and reducing the dosage frequency. boc-t4 can also serve as a tool for studying the role of thyroxine in various physiological processes. Group: Amino acids. Alternative Names: N-(tert-Butyloxy)carbonyl-L-thyroxine, Boc-T4. CAS No. 88404-22-2. Molecular formula: C20H19I4NO6. Mole weight: 877. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-3-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodophenyl]-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid. Canonical SMILES: CC (C) (C)OC (=O)N[C@@H] (CC1=CC (=C (C (=C1)I)OC2=CC (=C (C (=C2)I)O)I)I)C (=O)O. Catalog: ACM88404222. | |
| Boc-L-tyr(bzl)-chn2 | Heterocyclic Organic Compound. Alternative Names: Boc-L-Tyr(Bzl)-CHN2;N-alpha-tert-Butyloxycarbonyl-O-benzyl-L-tyrosine-diazomethane. CAS No. 114645-18-0. Molecular formula: C22H25N3O4. Mole weight: 395.45. Catalog: ACM114645180. | |
| Boc-Lys-OH | Derivative of synthesis of N-α-Boc-protected lysine derivatives. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Lys-OH, N-α-t.-Boc-L-lysine. CAS No. 13734-28-6. Molecular formula: C11H22N2O4. Mole weight: 246.3. Purity: TLC major spot. Catalog: ACM13734286. | |
| Boc-Lys(Z)-OH | Building block for introduction of lysine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Lys(Z)-OH, N-α-t.-Boc-N-ε-benzyloxycarbonyl-L-lysine. CAS No. 2389-45-9. Mole weight: 380.44. Catalog: ACM2389459. | |
| Boc-Met(O)-OH | Standard building block for introduction of methionine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Met(O)-OH, N-α-t.-Boc-L-methionine-DL-sulfoxide. CAS No. 34805-21-5. Mole weight: 265.33. Catalog: ACM34805215. | |
| Boc-Nalpha-methyl-N-im-trityl-L-histidine | Boc-Nalpha-methyl-N-im-trityl-L-histidine is a compound that is widely used in the fields of chemistry and biochemistry. It is a derivative of the natural amino acid L-histidine, and is commonly referred to as Trt-His(Me)-OH. The compound is characterized by the presence of a protecting group known as Boc, which makes it stable and easy to handle. This protective group can be removed under mild conditions, enabling the incorporation of Boc-Nalpha-methyl-N-im-trityl-L-histidine into complex molecules. The compound is used in a variety of research applications including peptide synthesis, drug discovery, and biological studies. Uses: Boc-nalpha-methyl-n-im-trityl-l-histidine has a wide range of applications in scientific research. it can be used in peptide synthesis to increase the solubility and stability of peptides. the compound can also be used as a protecting group during peptide synthesis to ensure the correct sequence of amino acids. additionally, boc-nalpha-methyl-n-im-trityl-l-histidine has been used in the developmen. Group: Amino acids. Alternative Names: N-Methyl-N-{[(2-methyl-2-propanyl)oxy]carbonyl}-1-tritylhistidine. CAS No. 1217610-35-9. Molecular formula: C31H33N3O4. Mole weight: 511.6. Purity: Peak Area by HPLC ≥95%. IUPACName: (2S)-2-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]-3-(1-tritylimidazol-4-yl)propanoic acid. Canonical SMILES: CC (C) (C)OC (=O)N (C)C (CC1=CN (C=N1 | |
| Boc-Nle-OH. DCHA | Standard building block for introduction of norleucine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Nle-OH. DCHA, N-α-t.-Boc-L-norleucine dicyclohexylammonium salt. CAS No. 21947-32-0. Mole weight: 412.61. Catalog: ACM21947320. | |
| Boc-N-Me-Ala-OH | Standard building block for introduction of alanine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-N-Me-Ala-OH, N-α-t.-Boc-N-α-methyl-L-alanine. CAS No. 16948-16-6. Mole weight: 203.24. Catalog: ACM16948166. | |
| Boc-N-Me-Val-OH | Standard building block for introduction of valine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-N-Me-Val-OH, N-α-t.-Boc-N-α-methyl-L-valine. CAS No. 45170-31-8. Mole weight: 231.29. Catalog: ACM45170318. | |
| Boc-Nva-OH | Standard building block for introduction of norvaline amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Nva-OH, N-α-t.-Boc-L-norvaline. CAS No. 53308-95-5. Mole weight: 217.26. Catalog: ACM53308955. | |
| Boc-O-benzyl-L-serine N,o-dimethylhydroxamide | Heterocyclic Organic Compound. CAS No. 115186-34-0. Molecular formula: C17H26N2O5. Mole weight: 338.4. Purity: 0.95. Catalog: ACM115186340. | |
| Boc-Orn(Z)-OH | Standard building block for introduction of ornithine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Orn(Z)-OH, N-α-t.-Boc-N-δ-benzyloxycarbonyl-L-ornithine. CAS No. 2480-93-5. Mole weight: 366.41. Catalog: ACM2480935. | |
| Boc-phe(2-cl)-oh | Heterocyclic Organic Compound. CAS No. 114293-02-8. Molecular formula: C14H18ClNO4. Purity: 0.96. Catalog: ACM114293028. | |
| Boc-Phe-OH | Standard building block for introduction of phenylalanine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Phe-OH, N-α-t.-Boc-L-phenylalanine. CAS No. 13734-34-4. Mole weight: 265.3. Catalog: ACM13734344-1. | |
| Boc-phe-phe-oh | Heterocyclic Organic Compound. Alternative Names: BOC-PHE-PSI(CH2NH)-PHE-OH;BOC-PHE-Y(CH2NH)-PHE-OH;BOC-PHE-(R)-PHE-OH;RARECHEM EM WB 0264. CAS No. 114290-82-3. Molecular formula: C23H30N2O4. Mole weight: 398.5. Purity: 0.96. IUPACName: (2S)-2-[[(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropyl]amino]-3-phenylpropanoicacid. Canonical SMILES: CC (C) (C)OC (=O)NC (CC1=CC=CC=C1)CNC (CC2=CC=CC=C2)C (=O)O. Catalog: ACM114290823. | |
| Boc-Phg-OH | Standard building block for introduction of phenylglycine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Phg-OH, N-α-t.-Boc-L-phenylglycine. CAS No. 2900-27-8. Mole weight: 251.28. Catalog: ACM2900278. | |
| Boc-Pro-OH | Standard building block for introduction of proline amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Pro-OH, N-α-t.-Boc-L-proline. CAS No. 15761-39-4. Mole weight: 215.25. Catalog: ACM15761394. | |
| Boc-Sar-OH | Standard building block for introduction of sarcosine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Sar-OH, N-α-t.-Boc-sarcosine. CAS No. 13734-36-6. Mole weight: 189.21. Catalog: ACM13734366-1. | |
| Boc-Ser(Bzl)-OH | Standard building block for introduction of serine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Ser(Bzl)-OH, N-α-t.-Boc-O-benzyl-L-serine. CAS No. 23680-31-1. Mole weight: 295.33. Catalog: ACM23680311. | |
| Boc-Ser-OH | N-α-Boc protection serine derivative with an unprotected hydroxyl group. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Ser-OH, N-α-t.-Boc-L-serine. CAS No. 3262-72-4. Mole weight: 205.21. Catalog: ACM3262724. | |
| Boc-s-methyl-L-penicillamine dicyclohexylammonium salt | Heterocyclic Organic Compound. Alternative Names: 112898-23-4, Dicyclohexylamine (R)-2-((tert-butoxycarbonyl)amino)-3-methyl-3-(methylthio)butanoate, BOC-PEN(ME)-OH DCHA, SCHEMBL6385080, MolPort-020-004-675, AKOS024463258, AK162599, ST24046497, K-0979. CAS No. 112898-23-4. Molecular formula: C11H21NO4S·C12H23N. Mole weight: 444.7. Purity: 0.96. IUPACName: N-cyclohexylcyclohexanamine;(2R)-3-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-methylsulfanylbutanoic acid. Canonical SMILES: CC(C)(C)OC(=O)NC(C(=O)O)C(C)(C)SC. C1CCC(CC1)NC2CCCCC2. Catalog: ACM112898234. | |
| Boc-ß-Ala-OH | Standard building block for introduction of β-alanine amino-acid residues by Boc SPPS. Uses: Boc-ß-ala-oh novabiochem®. cas 3303-84-2, molar mass 189.21 g/mol. Group: Amino acids. Alternative Names: Boc-ß-Ala-OH, N-β-t.-Boc-β-alanine. CAS No. 3303-84-2. Mole weight: 189.21. Catalog: ACM3303842. | |
| Boc-Thr(Bzl)-OH | Standard building block for introduction of threonine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Thr(Bzl)-OH, N-α-t.-Boc-O-benzyl-L-threonine. CAS No. 15260-10-3. Mole weight: 309.36. Catalog: ACM15260103. | |
| Boc-Thr-OH | Derivative of synthesis of side-chain modified glutamic acid derivatives. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Thr-OH, N-α-t.-Boc-L-threonine. CAS No. 2592-18-9. Mole weight: 219.23. Catalog: ACM2592189. | |
| Boc-Trp(Boc)-OH | N-in-Boc protection limits reattachment and leads to higher cleavage yields of C-terminal Trp-containing peptides. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Trp(Boc)-OH, N-α-t.-Boc-N-in-t.-Boc-L-trypophan. CAS No. 144599-95-1. Mole weight: 404.46. Catalog: ACM144599951. | |
| Boc-Trp(For)-OH | Standard building block for introduction of tryptophan by Boc SPPS. The formyl group is stable to standard high HF cleavage but can be removed by HF containing thiophenol. The formyl group can also be removed with piperidine in DMF prior to HF cleavage. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Trp(For)-OH, N-α-t.-Boc-N-in-formyl-L-tryptophan. CAS No. 47355-10-2. Mole weight: 332.35. Catalog: ACM47355102. | |
| Boc-Tyr(Me)-OH | Standard building block for introduction of O-methyl-tyrosine amino-acid residues by Boc SPPS. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Boc-Tyr(Me)-OH, N-α-t.-Boc-O-methyl-L-tyrosine, N-α-t.-Boc-p-methoxy-L-phenylalanine. CAS No. 53267-93-9. Molecular formula: C15H21NO5. Mole weight: 295.33. Catalog: ACM53267939. | |
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