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| Product | Description | |
|---|---|---|
| 2,3,5-Tri-O-benzyl-D-arabinofuranose | 2,3,5-Tri-O-benzyl-D-arabinofuranose is a biomedical intermediate commonly used in nucleoside synthesis. It is instrumental in the research and development of drugs treating a range of viral diseases, including HIV and Hepatitis. Synonyms: 2,3,5-Tri-O-benzyl-D-arabinofuranose; 160549-10-0; 37776-25-3; (3S,4R,5R)-3,4-Bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-ol; 2,3,5-Tri-O-benzyl-D-arabinofurannose; (3S,4R,5R)-3,4-bis(phenylmethoxy)-5-(phenylmethoxymethyl)oxolan-2-ol; SCHEMBL1561732; DTXSID10453669; NAQUAXSCBJPECG-DYXQDRAXSA-N; MFCD00080813; AKOS027383188; BS-16028; D82222; 2,3,5-tris-O-(phenylmethyl)-D-arabinofuranose; 2,3,5-Tri-O-benzyl-alpha/beta-D-arabinofuranose; A847918; W-202550; (3S,4R,5R)-3,4-bis(benzyloxy)-5-(benzyloxymethyl)-tetrahydrofuran-2-ol; (3S,4R,5R)-3,4-bis(benzyloxy)-5-(benzyloxymethyl)tetrahydrofuran-2-ol. CAS No. 160549-10-0. Molecular formula: C26H28O5. Mole weight: 420.5. |  |
| 2,3,5-Tri-O-benzyl-D-arabinofuranose | 2,3,5-Tri-O-benzyl-D-arabinofuranose is an aldopentose sugar that functions as an intermediate in the synthesis of phosphono analog of N-acetyl-α-D-mannosamine 1-phosphate from D-arabinose. Group: Biochemicals. Grades: Highly Purified. CAS No. 160549-10-0. Pack Sizes: 500mg, 1g. Molecular Formula: C26H28O5. US Biological Life Sciences. |  Worldwide |
| 2,3,5-Tri-O-benzyl-1-O-(4-nitrobenzoyl)-D-arabinofuranose | 2,3,5-Tri-O-benzyl-1-O-(4-nitrobenzoyl)-D-arabinofuranose, a fundamental compound extensively employed in the biomedical sector, exhibits remarkable significance. Its distinct chemical structure renders it an indispensable reagent in the synthesis of diverse pharmaceutical agents. This compound assumes a pivotal function in crafting drugs that specifically combat diseases like cancer, inflammatory disorders, and viral infections. Synonyms: 4-Nitrobenzoate 2,3,5-tri-O-benzyl-D-arabinofuranose. CAS No. 52522-49-3. Molecular formula: C33H31NO8. Mole weight: 569.6. | |
| 2,3,5-Tri-O-benzyl-D-arabinose | 2,3,5-Tri-O-benzyl-D-arabinose, an indispensable compound in the biomedical field, serves as a fundamental building block for the synthesis of assorted pharmaceuticals and substances. Its exceptional molecular structure renders it crucial in the advancement of therapeutic solutions for ailments such as cancer, viral infections, and neurological disorders. Synonyms: 2,3,5-Tri-O-benzyl-D-arabinofuranose; 160549-10-0; 37776-25-3; (3S,4R,5R)-3,4-Bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-ol; 2,3,5-Tri-O-benzyl-D-arabinofurannose; (3S,4R,5R)-3,4-bis(phenylmethoxy)-5-(phenylmethoxymethyl)oxolan-2-ol; SCHEMBL1561732; DTXSID10453669; NAQUAXSCBJPECG-DYXQDRAXSA-N; MFCD00080813; AKOS027383188; BS-16028; D82222; 2,3,5-tris-O-(phenylmethyl)-D-arabinofuranose; 2,3,5-Tri-O-benzyl-alpha/beta-D-arabinofuranose; A847918; W-202550; (3S,4R,5R)-3,4-bis(benzyloxy)-5-(benzyloxymethyl)-tetrahydrofuran-2-ol; (3S,4R,5R)-3,4-bis(benzyloxy)-5-(benzyloxymethyl)tetrahydrofuran-2-ol. CAS No. 37776-25-3. Molecular formula: C26H28O5. Mole weight: 420.505. | |
| b-L-Arabinofuranose,2,3,5-tris-O-(phenylmethyl)- | b-L-Arabinofuranose,2,3,5-tris-O-(phenylmethyl)-. Uses: Designed for use in research and industrial production. Additional or Alternative Names: T8255_SIGMA, NSC81026, MolPort-003-959-809, CID255457, NSC232028, 2,3,5-Tri-O-benzyl-beta-D-arabinofuranose, 2,3,5-Tri-O-benzyl-D-arabinofuranose, 2,3,5-Tri-O-benzyl-beta-L-arabinofuranose, 60933-68-8, 89615-42-9. Product Category: Heterocyclic Organic Compound. CAS No. 89615-42-9. Molecular formula: C26H28O5. Mole weight: 420.5. Purity: 0.96. IUPACName: 3,4-bis(phenylmethoxy)-5-(phenylmethoxymethyl)oxolan-2-ol. Canonical SMILES: C1=CC=C(C=C1)COCC2C(C(C(O2)O)OCC3=CC=CC=C3)OCC4=CC=CC=C4. Density: 1.21g/cm³. Product ID: ACM89615429. Alfa Chemistry ISO 9001:2015 Certified. |  |
| 2,3,5-Tri-O-benzyl-D-arabinofuranosyl chloride | 2,3,5-Tri-O-benzyl-D-arabinofuranosyl chloride, a chemical compound and starting material for antiviral and antitumor drugs, boasts noteworthy therapeutic effects against cancers like leukemia and lymphoma. Its DNA synthesis inhibition property, coupled with its role in apoptosis promotion, make it a promising candidate in combating cancer. CAS No. 52554-29-7. Molecular formula: C26H27ClO4. Mole weight: 438.94. | |
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