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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 of ACETOBROMGLUCOSE

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

PubMed

TitleDatePubMed
Glucopyranosides derived from 6-aryl-5-cyano-2-(methylthio)pyrimidin-4(3H)ones.
2002
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
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 Sep 25
Synthesis and antimicrobial activity of some cyclic and acyclic nucleosides of thieno[2,3-d]pyrimidines.
2007
Ultrasound-assisted reaction of 2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl bromide with potassium salt of curcumin under PTC conditions.
2008 Apr
Synthesis and evaluation of antimicrobial activity of some pyrimidine glycosides.
2008 Sep
Synthesis and antimicrobial activity of some S-beta-D-glucosides of 4-mercaptopyrimidine.
2009 Sep
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:58:20 GMT 2023
Edited
by admin
on Sat Dec 16 10:58:20 GMT 2023
Record UNII
ETH4010665
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACETOBROMGLUCOSE
MI  
Common Name English
ACETOBROMGLUCOSE [MI]
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
Created by admin on Sat Dec 16 10:58:20 GMT 2023 , Edited by admin on Sat Dec 16 10:58:20 GMT 2023
PRIMARY
FDA UNII
ETH4010665
Created by admin on Sat Dec 16 10:58:20 GMT 2023 , Edited by admin on Sat Dec 16 10:58:20 GMT 2023
PRIMARY
PUBCHEM
101776
Created by admin on Sat Dec 16 10:58:20 GMT 2023 , Edited by admin on Sat Dec 16 10:58:20 GMT 2023
PRIMARY
CAS
572-09-8
Created by admin on Sat Dec 16 10:58:20 GMT 2023 , Edited by admin on Sat Dec 16 10:58:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID001031860
Created by admin on Sat Dec 16 10:58:20 GMT 2023 , Edited by admin on Sat Dec 16 10:58:20 GMT 2023
PRIMARY
MERCK INDEX
m1329
Created by admin on Sat Dec 16 10:58:20 GMT 2023 , Edited by admin on Sat Dec 16 10:58:20 GMT 2023
PRIMARY Merck Index