2-THIAZOLIDINIMINE, 3-(2-PHENYLETHENYL)-, (E)-

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	MOL RATIO 1 MOL RATIO (average)

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	1
Optical Activity	NONE

Approval Year

Substance Class	Chemical
Record UNII	60AQZ8W67M
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

3-((E)-2-PHENYLETHENYL)THIAZOLIDIN-2-IMINE

Preferred Name

English

2-THIAZOLIDINIMINE, 3-(2-PHENYLETHENYL)-, (E)-

Systematic Name

English

LEVAMISOLE HYDROCHLORIDE IMPURITY B [WHO-IP]

Common Name

English

LEVAMISOLE HYDROCHLORIDE IMPURITY B [EP IMPURITY]

Common Name

English

2-IMINO-3-STYRYLTHIAZOLIDINE, TRANS-

Systematic Name

English

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Code System

Code

Type

Description

CAS

37430-07-2

PRIMARY

PUBCHEM

20313825

PRIMARY

FDA UNII

60AQZ8W67M

PRIMARY

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Related Record

Type

Details


					2880D3468G

LEVAMISOLE

PARENT -> IMPURITY

Comments:

- for veterinary use - correction factor: for the calculation of content, multiply the peak area of impurity B by 1.7

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:

[<0.2] PERCENT PEAK AREA (limits)


					DL9055K809

LEVAMISOLE HYDROCHLORIDE

PARENT -> IMPURITY

Comments:

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%).

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

EP

Amount:

WEIGHT PERCENT [<0.2] % (limits)
peak value

Showing 1 to 2 of 2 entries

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