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Details

Stereochemistry EPIMERIC
Molecular Formula C16H19N3O6S
Molecular Weight 381.404
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-((R)-(((2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETYL)AMINO)CARBOXYMETHYL)-5-METHYL-5,6-DIHYDRO-2H-1,3-THIAZINE-4-CARBOXYLIC ACID, (2R,5RS)-

SMILES

CC1CS[C@@H](N=C1C(O)=O)[C@H](NC(=O)[C@H](N)C2=CC=C(O)C=C2)C(O)=O

InChI

InChIKey=SGGNURHBTCABDM-FBTHNIEXSA-N
InChI=1S/C16H19N3O6S/c1-7-6-26-14(19-11(7)15(22)23)12(16(24)25)18-13(21)10(17)8-2-4-9(20)5-3-8/h2-5,7,10,12,14,20H,6,17H2,1H3,(H,18,21)(H,22,23)(H,24,25)/t7?,10-,12+,14-/m1/s1

HIDE SMILES / InChI

Molecular Formula C16H19N3O6S
Molecular Weight 381.404
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 3 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:34:49 GMT 2025
Edited
by admin
on Mon Mar 31 21:34:49 GMT 2025
Record UNII
V90Y86LJ0K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-((R)-(((2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETYL)AMINO)CARBOXYMETHYL)-5-METHYL-5,6-DIHYDRO-2H-1,3-THIAZINE-4-CARBOXYLIC ACID, (2R,5RS)-
Common Name English
CEFADROXIL IMPURITY C [EP IMPURITY]
Preferred Name English
(2R,5RS)-2-((R)-(((2R)-2-AMINO-2-(4-HYDROXYPHENYL)ACETYL)AMINO)CARBOXYMETHYL)-5-METHYL-5,6-DIHYDRO-2H-1,3-THIAZINE-4-CARBOXYLIC ACID
Systematic Name English
CEFADROXIL MONOHYDRATE IMPURITY C [EP IMPURITY]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID70163595
Created by admin on Mon Mar 31 21:34:49 GMT 2025 , Edited by admin on Mon Mar 31 21:34:49 GMT 2025
PRIMARY
CAS
147103-96-6
Created by admin on Mon Mar 31 21:34:49 GMT 2025 , Edited by admin on Mon Mar 31 21:34:49 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
FDA UNII
V90Y86LJ0K
Created by admin on Mon Mar 31 21:34:49 GMT 2025 , Edited by admin on Mon Mar 31 21:34:49 GMT 2025
PRIMARY
PUBCHEM
71587521
Created by admin on Mon Mar 31 21:34:49 GMT 2025 , Edited by admin on Mon Mar 31 21:34:49 GMT 2025
PRIMARY