Home Other Building Blocks 2,3,4,6-Tetra-O-acetyl-alpha-D-glucopyranosyl bromide

2,3,4,6-Tetra-O-acetyl-alpha-D-glucopyranosyl bromide

CAS No.:
572-09-8
Catalog Number:
AG00391Z
Molecular Formula:
C14H19BrO9
Molecular Weight:
411.1993
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$13
- +
5g
98%
In Stock USA
United States
$25
- +
25g
98%
In Stock USA
United States
$58
- +
100g
98%
In Stock USA
United States
$188
- +
500g
98%
In Stock USA
United States
$750
- +
Product Description
Catalog Number:
AG00391Z
Chemical Name:
2,3,4,6-Tetra-O-acetyl-alpha-D-glucopyranosyl bromide
CAS Number:
572-09-8
Molecular Formula:
C14H19BrO9
Molecular Weight:
411.1993
MDL Number:
MFCD00063254
IUPAC Name:
[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-bromooxan-2-yl]methyl acetate
InChI:
InChI=1S/C14H19BrO9/c1-6(16)20-5-10-11(21-7(2)17)12(22-8(3)18)13(14(15)24-10)23-9(4)19/h10-14H,5H2,1-4H3/t10-,11-,12+,13-,14+/m1/s1
InChI Key:
CYAYKKUWALRRPA-RGDJUOJXSA-N
SMILES:
CC(=O)OC[C@H]1O[C@H](Br)[C@@H]([C@H]([C@@H]1OC(=O)C)OC(=O)C)OC(=O)C
EC Number:
209-339-0
UNII:
ETH4010665
Properties
Complexity:
507  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
5  
Defined Bond Stereocenter Count:
0
Exact Mass:
410.021g/mol
Formal Charge:
0
Heavy Atom Count:
24  
Hydrogen Bond Acceptor Count:
9  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
411.201g/mol
Monoisotopic Mass:
410.021g/mol
Rotatable Bond Count:
9  
Topological Polar Surface Area:
114A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5  
Literature
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Selective formation of glycosidic linkages of N-unsubstituted 4-hydroxyquinolin-2-(1H)-ones. Carbohydrate research 20100419
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Glycosidation of 2,5-anhydro-3,4-di-O-benzyl-D-mannitol with different glucopyranosyl donors: a comparative study. Carbohydrate research 20060501
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Synthesis of some new 1,3/ or 1,4-bis(glucopyranosyl-1,2,4-triazol-5-ylthio)propanes/ or butanes as potential antimicrobial agents. Nucleosides, nucleotides & nucleic acids 20050101
Synthesis of some novel 6-benzyl(or substituted benzyl)-2-beta-D-glucopyranosyl-1,2,4-triazolo[4,3-b][1,2,4]triazines as potential antimicrobial chemotherapeutics. Nucleosides, nucleotides & nucleic acids 20040101
Towards alpha- or beta-D-C-glycosyl compounds by tin-catalyzed addition of glycosyl radicals to acrylonitrile and vinylphosphonate, and flexible reduction of tetra-O-acetyl-alpha-D-glucopyranosyl bromide with cyanoborohydride. Carbohydrate research 20021008
Glucopyranosides derived from 6-aryl-5-cyano-2-(methylthio)pyrimidin-4(3H)ones. Nucleosides, nucleotides & nucleic acids 20020101
Synthesis of 2-thiohydantoins and their S-glucosylated derivatives as potential antiviral and antitumor agents. Nucleosides, nucleotides & nucleic acids 20010901
Glycosylation of 2-thiohydantoin derivatives. Synthesis of some novel S-alkylated and S-glucosylated hydantoins. Carbohydrate research 20010423
Properties