ACETOBROMGLUCOSE

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C14H19BrO9
Molecular Weight	411.199
Optical Activity	UNSPECIFIED
Defined Stereocenters	5 / 5
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC(=O)OC[C@H]1O[C@H](Br)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

InChI

InChIKey=CYAYKKUWALRRPA-RGDJUOJXSA-N

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

HIDE SMILES / InChI

Molecular Formula	C14H19BrO9
Molecular Weight	411.199
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	5 / 5
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

Title	Date	PubMed
Selective formation of glycosidic linkages of N-unsubstituted 4-hydroxyquinolin-2-(1H)-ones.	2010-04-19	20206337
Glycosylation, sugar hydrazones, and antimicrobial evaluation of some 6-substituted-1,2,4-triazines.	2010-01	20391193
Antiviral and antischistosomal evaluation of newly synthesized thioglycosides and their acyclic analogues.	2009-10-02	19791497
Synthesis and antimicrobial activity of some S-beta-D-glucosides of 4-mercaptopyrimidine.	2009-09	20183622
Synthesis and evaluation of antimicrobial activity of some pyrimidine glycosides.	2008-09	18711668
Ultrasound-assisted reaction of 2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl bromide with potassium salt of curcumin under PTC conditions.	2008-04	17981492
Synthesis and antimicrobial activity of some cyclic and acyclic nucleosides of thieno[2,3-d]pyrimidines.	2007	17479433
Novel simple efficient synthetic approach toward 6-substituted-2H-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole-3-thiones and first synthesis and biological evaluation of N-and S-beta-D-glucosides of the[1,2,4]triazolo [3,4-b][1,3,4]thiadiazole ring system.	2007	17479431
Efficient synthesis, structure, and antimicrobial activity of some novel N- and S-beta-D-glucosides of 5-pyridin-3-yl-1,2,4-triazoles.	2006-09-25	16839524
Synthesis of 6-O-methyl ether of Scorzocreticin and Scorzocreticoside I, metabolites from Sorzonera cretica.	2006-07-26	16864457
Glycosidation of 2,5-anhydro-3,4-di-O-benzyl-D-mannitol with different glucopyranosyl donors: a comparative study.	2006-05-01	16473342
Synthesis of some new 1,3/ or 1,4-bis(glucopyranosyl-1,2,4-triazol-5-ylthio)propanes/ or butanes as potential antimicrobial agents.	2005	16252672
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.	2004	15628747
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.	2002-10-08	12423963
Glucopyranosides derived from 6-aryl-5-cyano-2-(methylthio)pyrimidin-4(3H)ones.	2002	11991146
Synthesis of 2-thiohydantoins and their S-glucosylated derivatives as potential antiviral and antitumor agents.	2001-09	11580198
Glycosylation of 2-thiohydantoin derivatives. Synthesis of some novel S-alkylated and S-glucosylated hydantoins.	2001-04-23	11398987

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 23:32:48 GMT 2025` Edited by `admin` on `Mon Mar 31 23:32:48 GMT 2025`
Record UNII	ETH4010665
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

ACETOBROMGLUCOSE [MI]

Preferred Name

English

ACETOBROMGLUCOSE

Common Name

English

D-ACETOBROMOGLUCOSE

Common Name

English

ACETOBROMO-.ALPHA.-D-GLUCOSE

Common Name

English

ACETYLBROMOGLUCOSE

Systematic Name

English

2,3,4,6-TETRAACETYL-.ALPHA.-D-GLUCOPYRANOSYL BROMIDE

Systematic Name

English

Code System Code Type Description

ECHA (EC/EINECS)

209-339-0