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Details

Stereochemistry RACEMIC
Molecular Formula C10H12O4S
Molecular Weight 228.265
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GLYCIDYL TOSYLATE, (±)-

SMILES

CC1=CC=C(C=C1)S(=O)(=O)OCC2CO2

InChI

InChIKey=NOQXXYIGRPAZJC-UHFFFAOYSA-N
InChI=1S/C10H12O4S/c1-8-2-4-10(5-3-8)15(11,12)14-7-9-6-13-9/h2-5,9H,6-7H2,1H3

HIDE SMILES / InChI

Molecular Formula C10H12O4S
Molecular Weight 228.265
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 12:43:31 GMT 2023
Edited
by admin
on Sat Dec 16 12:43:31 GMT 2023
Record UNII
QT428577JZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GLYCIDYL TOSYLATE, (±)-
Systematic Name English
NSC-143322
Code English
GLYCIDOL P-TOLUENESULFONATE
Common Name English
2-OXIRANEMETHANOL, 2-(4-METHYLBENZENESULFONATE)
Systematic Name English
(±)-GLYCIDYL TOSYLATE
Systematic Name English
2,3-EPOXY-1-PROPYL P-TOLUENESULFONATE
Systematic Name English
2,3-EPOXYPROPYL TOSYLATE
Systematic Name English
Code System Code Type Description
FDA UNII
QT428577JZ
Created by admin on Sat Dec 16 12:43:31 GMT 2023 , Edited by admin on Sat Dec 16 12:43:31 GMT 2023
PRIMARY
CAS
6746-81-2
Created by admin on Sat Dec 16 12:43:31 GMT 2023 , Edited by admin on Sat Dec 16 12:43:31 GMT 2023
PRIMARY
PUBCHEM
160868
Created by admin on Sat Dec 16 12:43:31 GMT 2023 , Edited by admin on Sat Dec 16 12:43:31 GMT 2023
PRIMARY
NSC
143322
Created by admin on Sat Dec 16 12:43:31 GMT 2023 , Edited by admin on Sat Dec 16 12:43:31 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE