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Details

Stereochemistry ACHIRAL
Molecular Formula C11H12N2S
Molecular Weight 204.291
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of 2-THIAZOLIDINIMINE, 3-(2-PHENYLETHENYL)-, (E)-

SMILES

N=C1SCCN1\C=C\C2=CC=CC=C2

InChI

InChIKey=VTWWXGPFQZXGGE-WQAKAUOBSA-N
InChI=1S/C11H12N2S/c12-11-13(8-9-14-11)7-6-10-4-2-1-3-5-10/h1-7,12H,8-9H2/b7-6+,12-11?

HIDE SMILES / InChI

Molecular Formula C11H12N2S
Molecular Weight 204.291
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 09:59:52 GMT 2023
Edited
by admin
on Sat Dec 16 09:59:52 GMT 2023
Record UNII
60AQZ8W67M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-THIAZOLIDINIMINE, 3-(2-PHENYLETHENYL)-, (E)-
Systematic Name English
LEVAMISOLE HYDROCHLORIDE IMPURITY B [WHO-IP]
Common Name English
3-((E)-2-PHENYLETHENYL)THIAZOLIDIN-2-IMINE
Systematic Name English
LEVAMISOLE HYDROCHLORIDE IMPURITY B [EP IMPURITY]
Common Name English
2-IMINO-3-STYRYLTHIAZOLIDINE, TRANS-
Systematic Name English
TRANS-2-IMINO-3-STYRYLTHIAZOLIDINE
Systematic Name English
3-((E)-2-PHENYLETHENYL)THIAZOLIDIN-2-IMINE [WHO-IP]
Common Name English
LEVAMISOLE FOR VETERINARY USE IMPURITY B [EP IMPURITY]
Common Name English
Code System Code Type Description
CAS
37430-07-2
Created by admin on Sat Dec 16 09:59:52 GMT 2023 , Edited by admin on Sat Dec 16 09:59:52 GMT 2023
PRIMARY
PUBCHEM
20313825
Created by admin on Sat Dec 16 09:59:52 GMT 2023 , Edited by admin on Sat Dec 16 09:59:52 GMT 2023
PRIMARY
FDA UNII
60AQZ8W67M
Created by admin on Sat Dec 16 09:59:52 GMT 2023 , Edited by admin on Sat Dec 16 09:59:52 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
- for veterinary use - correction factor: for the calculation of content, multiply the peak area of impurity B by 1.7
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
The chromatogram obtained with solution (1) may show peaks due to the following impurities eluting at the following relative retention with reference to levamisole (retention time about 3.5 minutes): impurity B about 1.4. In the chromatogram obtained with solution (1): ?the area of any peak corresponding to impurity B, when multiplied by a correction factor of 1.7, is not greater than 2 times the area of the peak due to levamisole in the chromatogram obtained with solution (4) (0.2%).
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP