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Details

Stereochemistry ABSOLUTE
Molecular Formula C16H17N3O7S2
Molecular Weight 427.452
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-[(carbamoyloxy)methyl]-7-methoxy-8-oxo-7-[2-(thiophen-2-yl)acetamido]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, (6S,7R)-

SMILES

CO[C@@]2(NC(=O)CC1=CC=CS1)[C@@H]3SCC(COC(N)=O)=C(N3C2=O)C(O)=O

InChI

InChIKey=WZOZEZRFJCJXNZ-GOEBONIOSA-N
InChI=1S/C16H17N3O7S2/c1-25-16(18-10(20)5-9-3-2-4-27-9)13(23)19-11(12(21)22)8(6-26-15(17)24)7-28-14(16)19/h2-4,14H,5-7H2,1H3,(H2,17,24)(H,18,20)(H,21,22)/t14-,16+/m0/s1

HIDE SMILES / InChI

Molecular Formula C16H17N3O7S2
Molecular Weight 427.452
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Wed Apr 02 17:40:42 GMT 2025
Edited
by admin
on Wed Apr 02 17:40:42 GMT 2025
Record UNII
Q2JN2A726P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(6S,7R)-3-[(carbamoyloxy)methyl]-7-methoxy-8-oxo-7-[2-(thiophen-2-yl)acetamido]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Preferred Name English
3-[(carbamoyloxy)methyl]-7-methoxy-8-oxo-7-[2-(thiophen-2-yl)acetamido]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, (6S,7R)-
Systematic Name English
5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, 3-[[(aminocarbonyl)oxy]methyl]-7-methoxy-8-oxo-7-[(2-thienylacetyl)amino]-, (6S-cis)-
Systematic Name English
(6S-cis)-3-[[(aminocarbonyl)oxy]methyl]-7-methoxy-8-oxo-7-[(2-thienylacetyl)amino]-5-Thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
Systematic Name English
Code System Code Type Description
PUBCHEM
36552
Created by admin on Wed Apr 02 17:40:42 GMT 2025 , Edited by admin on Wed Apr 02 17:40:42 GMT 2025
PRIMARY
FDA UNII
Q2JN2A726P
Created by admin on Wed Apr 02 17:40:42 GMT 2025 , Edited by admin on Wed Apr 02 17:40:42 GMT 2025
PRIMARY
CAS
56082-95-2
Created by admin on Wed Apr 02 17:40:42 GMT 2025 , Edited by admin on Wed Apr 02 17:40:42 GMT 2025
PRIMARY