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
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
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 |
---|---|---|
Glucopyranosides derived from 6-aryl-5-cyano-2-(methylthio)pyrimidin-4(3H)ones. | 2002 |
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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. | 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
Edited
Sat Dec 16 10:58:20 GMT 2023
by
admin
on
Sat Dec 16 10:58:20 GMT 2023
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Record UNII |
ETH4010665
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Record Status |
Validated (UNII)
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Record Version |
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209-339-0
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ETH4010665
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101776
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572-09-8
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DTXSID001031860
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admin on Sat Dec 16 10:58:20 GMT 2023 , Edited by admin on Sat Dec 16 10:58:20 GMT 2023
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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
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PRIMARY | Merck Index |