
CAS 13039-75-3: 5-Deoxy-D-ribose
Formula:C5H10O4
InChI:InChI=1/C5H10O4/c1-3(7)5(9)4(8)2-6/h2-5,7-9H,1H3/t3-,4+,5-/m1/s1
Synonyms:- (2R,3R,4R)-2,3,4-trihydroxypentanal
- 5-deoxy-beta-D-ribofuranose
Sort by
Found 5 products.
5-Deoxy-D-ribose
CAS:Controlled ProductApplications Used in the process for preparing Capecitabine and β-trialkyl carbonate nucleosides. References Shimma, N., et al.: Bioorg. Med. Chem., 8, 1697 (2000),Formula:C5H10O4Color and Shape:NeatMolecular weight:134.135-Deoxy-D-ribose
CAS:Formula:C5H10O4Purity:(TLC) ≥ 98%Color and Shape:Colourless to light-yellow liquidMolecular weight:134.135-Deoxy-D-ribose
CAS:5-Deoxy-D-ribose is a molecule that is an intermediate in the shikimate pathway, which produces the aromatic amino acids. 5-Deoxy-D-ribose can be synthesized from D-ribose and shikimic acid. The biosynthesis of 5-deoxy-D-ribose is catalyzed by the enzyme ribose 5'-phosphate kinase, which converts ribose 5'-phosphate to 5-deoxy--D--ribose phosphate. This reaction requires ATP as a source of energy, and it is inhibited by phosphoribosyl pyrophosphate (PRPP). The asymmetric synthesis of 5-deoxy--D--ribose has been achieved with a chiral Lewis acid catalyst. The molecular structure of 5-deoxy--D--ribose has been determined by NMR spectroscopy. Shikimate pathways are present in mammalian cells, but not in plants or bacteria.Formula:C5H10O4Purity:Min. 95 Area-%Color and Shape:Orange Clear LiquidMolecular weight:134.13 g/mol