CAS 78963-40-3
:(2S,3R,4S,5R)-2,3,4,5-Tetrahydroxycyclohexanone
Description:
(2S,3R,4S,5R)-2,3,4,5-Tetrahydroxycyclohexanone, with the CAS number 78963-40-3, is a cyclic organic compound characterized by its six-membered cyclohexane ring that contains four hydroxyl (-OH) groups and one ketone (C=O) functional group. This compound exhibits chirality due to the presence of multiple stereocenters, resulting in specific stereoisomer configurations. The hydroxyl groups contribute to its hydrophilicity, making it soluble in water and capable of forming hydrogen bonds, which can influence its reactivity and interactions with other molecules. The ketone functional group adds to its reactivity, allowing it to participate in various chemical reactions, such as oxidation and reduction. This compound is of interest in organic synthesis and may have applications in pharmaceuticals or as a chiral building block in the synthesis of more complex molecules. Its specific stereochemistry can significantly affect its biological activity and properties, making it a subject of study in fields such as medicinal chemistry and biochemistry.
Formula:C6H10O5
InChI:InChI=1S/C6H10O5/c7-2-1-3(8)5(10)6(11)4(2)9/h2,4-7,9-11H,1H2/t2-,4+,5-,6-/m1/s1
InChI key:InChIKey=GZYCZKBRQBKGJW-FSZQNWAESA-N
SMILES:O[C@@H]1[C@@H](O)[C@H](O)C(=O)C[C@H]1O
Synonyms:- (-)-2-Deoxy-scyllo-inosose
- (2S,3R,4S,5R)-2,3,4,5-Tetrahydroxycyclohexanone
- Cyclohexanone, 2,3,4,5-tetrahydroxy-, (2S,3R,4S,5R)-
- (-)-Deoxy-scyllo-inosose
- Cyclohexanone, 2,3,4,5-tetrahydroxy-, [2S-(2α,3β,4α,5β)]-
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Found 3 products.
2-Deoxy-scyllo-inosose
CAS:<p>2-Deoxy-scyllo-inosose</p>Color and Shape:SolidMolecular weight:162.14g/mol2-Deoxy-scyllo-inosose
CAS:<p>2-Deoxy-scyllo-inosose is a biochemical with an unknown function. It is not a substrate for any known enzyme, but has been shown to be a substrate for the synthesis of corynebacterium glutamicum. The reaction mechanism of 2-deoxy-scyllo-inosose is still unclear, but it has been proposed that this molecule undergoes dehydration and then undergoes an acid catalyzed aldol cyclization to form 3-aminohexanol. This reaction produces fluorescence resonance energy transfer in group p2 subtilisin.<br>2DOS is also an antimicrobial agent which exhibits activity against Gram positive bacteria such as Streptococcus pyogenes, Enterococcus faecalis, and Bacillus subtilis.</p>Formula:C6H10O5Purity:Min. 95%Color and Shape:White PowderMolecular weight:162.14 g/mol
