CAS 20031-21-4 | α-D-Xylofuranose, 1,2-O-(1-methylethylidene)- | CAS Number 20031-21-4

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20031-21-4 | α-D-Xylofuranose, 1,2-O-(1-methylethylidene)-

CAS No: 20031-21-4 Catalog No: AG002COM MDL No:MFCD00063295

Product Description

Catalog Number:

AG002COM

Chemical Name:

α-D-Xylofuranose, 1,2-O-(1-methylethylidene)-

CAS Number:

20031-21-4

Molecular Formula:

C8H14O5

Molecular Weight:

190.1938

MDL Number:

MFCD00063295

IUPAC Name:

(3aR,5R,6S,6aR)-5-(hydroxymethyl)-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-ol

InChI:

InChI=1S/C8H14O5/c1-8(2)12-6-5(10)4(3-9)11-7(6)13-8/h4-7,9-10H,3H2,1-2H3/t4-,5+,6-,7-/m1/s1

InChI Key:

JAUQZVBVVJJRKM-XZBKPIIZSA-N

SMILES:

OC[C@H]1O[C@H]2[C@@H]([C@H]1O)OC(O2)(C)C

Properties

Complexity:

205

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

190.084g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

190.195g/mol

Monoisotopic Mass:

190.084g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

68.2A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

-0.4

Literature

Title	Journal
Efficient synthesis, structural characterization and anti-microbial activity of chiral aryl boronate esters of 1,2-O-isopropylidene-α-D-xylofuranose.	Bioorganic & medicinal chemistry letters 20110701
A short and practical synthesis of two Hagen's gland lactones.	Carbohydrate research 20090612
Novel D-xylose derivatives stimulate muscle glucose uptake by activating AMP-activated protein kinase alpha.	Journal of medicinal chemistry 20081225
Synthesis of highly condensed polycyclic carbohydrates by reaction of a spirocyclic enamino sulfonate derived from d-xylofuranose with bifunctional reagents.	The Journal of organic chemistry 20071207
A cyclic enamine derived from 1,2-O-isopropylidene-alpha-D-xylofuranose as a novel carbohydrate intermediate to achieve skeletal diversity.	The Journal of organic chemistry 20060915