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Details

Stereochemistry ACHIRAL
Molecular Formula C22H34N4O4S
Molecular Weight 450.595
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-(CYCLOHEXYLCARBAMOYL)-4-(2-((CYCLOHEXYLCARBAMOYL)AMINO)ETHYL)BENZENESULFONAMIDE

SMILES

O=C(NCCC1=CC=C(C=C1)S(=O)(=O)NC(=O)NC2CCCCC2)NC3CCCCC3

InChI

InChIKey=FYNBBKUBRFUWKU-UHFFFAOYSA-N
InChI=1S/C22H34N4O4S/c27-21(24-18-7-3-1-4-8-18)23-16-15-17-11-13-20(14-12-17)31(29,30)26-22(28)25-19-9-5-2-6-10-19/h11-14,18-19H,1-10,15-16H2,(H2,23,24,27)(H2,25,26,28)

HIDE SMILES / InChI

Molecular Formula C22H34N4O4S
Molecular Weight 450.595
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 08:54:15 UTC 2023
Edited
by admin
on Sat Dec 16 08:54:15 UTC 2023
Record UNII
4PC04VFC3Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-(CYCLOHEXYLCARBAMOYL)-4-(2-((CYCLOHEXYLCARBAMOYL)AMINO)ETHYL)BENZENESULFONAMIDE
Systematic Name English
GLIBENCLAMIDE IMPURITY C [EP IMPURITY]
Common Name English
GLIPIZIDE IMPURITY I [EP IMPURITY]
Common Name English
UREA, 1-CYCLOHEXYL-3-(P-((CYCLOHEXYLCARBAMOYL)SULFAMOYL)PHENETHYL)-
Common Name English
BENZENESULFONAMIDE, N-((CYCLOHEXYLAMINO)CARBONYL)-4-(2-(((CYCLOHEXYLAMINO)CARBONYL)AMINO)ETHYL)-
Systematic Name English
Code System Code Type Description
PUBCHEM
71315091
Created by admin on Sat Dec 16 08:54:15 UTC 2023 , Edited by admin on Sat Dec 16 08:54:15 UTC 2023
PRIMARY
FDA UNII
4PC04VFC3Y
Created by admin on Sat Dec 16 08:54:15 UTC 2023 , Edited by admin on Sat Dec 16 08:54:15 UTC 2023
PRIMARY
EPA CompTox
DTXSID90143511
Created by admin on Sat Dec 16 08:54:15 UTC 2023 , Edited by admin on Sat Dec 16 08:54:15 UTC 2023
PRIMARY
CAS
10079-35-3
Created by admin on Sat Dec 16 08:54:15 UTC 2023 , Edited by admin on Sat Dec 16 08:54:15 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
For the calculation of contents, multiply the peak areas by 2.1
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP