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Details

Stereochemistry RACEMIC
Molecular Formula C4H6N2O2S
Molecular Weight 146.168
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-Aminothiazoline-4-carboxylic acid

SMILES

NC1=NC(CS1)C(O)=O

InChI

InChIKey=VHPXSBIFWDAFMB-UHFFFAOYSA-N
InChI=1S/C4H6N2O2S/c5-4-6-2(1-9-4)3(7)8/h2H,1H2,(H2,5,6)(H,7,8)

HIDE SMILES / InChI

Molecular Formula C4H6N2O2S
Molecular Weight 146.168
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:56:19 GMT 2023
Edited
by admin
on Sat Dec 16 10:56:19 GMT 2023
Record UNII
48431VN59G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-Aminothiazoline-4-carboxylic acid
Systematic Name English
DL-2-AMINOTHIAZOLINE-4-CARBOXYLIC ACID
Systematic Name English
2-IMINOTHIAZOLIDINE-4-CARBOXYLIC ACID
Systematic Name English
DL-2-AMINO-2-THIAZOLIN-4-CARBOXYLIC ACID
Systematic Name English
4-THIAZOLECARBOXYLIC ACID, 2-AMINO-4,5-DIHYDRO-
Common Name English
NSC-25069
Code English
2-AMINO-2-THIAZOLINE-4-CARBOXYLIC ACID
Systematic Name English
DL-2-AMINO-.DELTA.2-THIAZOLINE-4-CARBOXYLIC ACID
Systematic Name English
2-THIAZOLINE-4-CARBOXYLIC ACID, 2-AMINO-
Systematic Name English
Code System Code Type Description
FDA UNII
48431VN59G
Created by admin on Sat Dec 16 10:56:20 GMT 2023 , Edited by admin on Sat Dec 16 10:56:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
218-433-0
Created by admin on Sat Dec 16 10:56:19 GMT 2023 , Edited by admin on Sat Dec 16 10:56:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID9024510
Created by admin on Sat Dec 16 10:56:19 GMT 2023 , Edited by admin on Sat Dec 16 10:56:19 GMT 2023
PRIMARY
WIKIPEDIA
2-Aminothiazoline-4-carboxylic acid
Created by admin on Sat Dec 16 10:56:20 GMT 2023 , Edited by admin on Sat Dec 16 10:56:20 GMT 2023
PRIMARY
PUBCHEM
16526
Created by admin on Sat Dec 16 10:56:20 GMT 2023 , Edited by admin on Sat Dec 16 10:56:20 GMT 2023
PRIMARY
NSC
25069
Created by admin on Sat Dec 16 10:56:20 GMT 2023 , Edited by admin on Sat Dec 16 10:56:20 GMT 2023
PRIMARY
CAS
2150-55-2
Created by admin on Sat Dec 16 10:56:19 GMT 2023 , Edited by admin on Sat Dec 16 10:56:19 GMT 2023
PRIMARY
CHEBI
64777
Created by admin on Sat Dec 16 10:56:19 GMT 2023 , Edited by admin on Sat Dec 16 10:56:19 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE