CAS 58871-06-0
:D-arabino-Hex-1-enitol, 1,5-anhydro-2-deoxy-, 3,6-dibenzoate
Description:
D-arabino-Hex-1-enitol, 1,5-anhydro-2-deoxy-, 3,6-dibenzoate, with CAS number 58871-06-0, is a chemical compound characterized by its unique structural features. It is a derivative of a sugar alcohol, specifically an anhydro sugar, which indicates the absence of a water molecule that typically forms during the condensation of sugars. The presence of the "dibenzoate" moiety suggests that the compound has two benzoate groups attached, which can influence its solubility, stability, and reactivity. This compound may exhibit properties typical of sugar derivatives, such as being a potential substrate for enzymatic reactions or serving as a building block in organic synthesis. Its structural configuration, including the hexene and anhydro functionalities, may impart specific stereochemical properties that could be relevant in biological systems or synthetic applications. Overall, the characteristics of this compound make it of interest in fields such as organic chemistry, biochemistry, and potentially in pharmaceutical applications.
Formula:C20H18O6
InChI:InChI=1S/C20H18O6/c21-18-16(26-20(23)15-9-5-2-6-10-15)11-12-24-17(18)13-25-19(22)14-7-3-1-4-8-14/h1-12,16-18,21H,13H2/t16-,17-,18+/m1/s1
InChI key:InChIKey=MXJFEWOUOTWSTM-KURKYZTESA-N
SMILES:O(C(=O)C1=CC=CC=C1)[C@H]2[C@H](O)[C@@H](COC(=O)C3=CC=CC=C3)OC=C2
Synonyms:- D-arabino-Hex-1-enitol, 1,5-anhydro-2-deoxy-, 3,6-dibenzoate
- 3,6-Di-O-benzoyl-D-glucal
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Found 4 products.
((2R,3S,4R)-4-(Benzoyloxy)-3-hydroxy-3,4-dihydro-2H-pyran-2-yl)methyl benzoate
CAS:Formula:C20H18O6Molecular weight:354.35333,6-Di-O-benzoyl-D-glucal
CAS:<p>3,6-Di-O-benzoyl-D-glucal</p>Color and Shape:SolidMolecular weight:354.35g/mol3,6-Di-O-benzoyl-D-glucal
CAS:<p>3,6-Di-O-benzoyl-D-glucal is a glycosylation reagent that can be used to modify proteins with oligosaccharides. It is a naturally occurring sugar that can be synthesized and modified for use in research. 3,6-Di-O-benzoyl-D-glucal has been shown to be effective in Click chemistry, which uses copper ions to produce reactive esters from alcohols and carboxylic acids. This reagent can also be used to fluorinate saccharides and sugars for high purity synthesis.</p>Purity:Min. 95%



