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Details

Stereochemistry ACHIRAL
Molecular Formula C12H15N3O
Molecular Weight 217.267
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-(2-KETO-1-BENZIMIDAZOLINYL)PIPERIDINE

SMILES

O=C1NC2=CC=CC=C2N1C3CCNCC3

InChI

InChIKey=BYNBAMHAURJNTR-UHFFFAOYSA-N
InChI=1S/C12H15N3O/c16-12-14-10-3-1-2-4-11(10)15(12)9-5-7-13-8-6-9/h1-4,9,13H,5-8H2,(H,14,16)

HIDE SMILES / InChI

Molecular Formula C12H15N3O
Molecular Weight 217.267
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 08:23:54 UTC 2023
Edited
by admin
on Sat Dec 16 08:23:54 UTC 2023
Record UNII
4RP0AED2PC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-(2-KETO-1-BENZIMIDAZOLINYL)PIPERIDINE
Systematic Name English
4-(2-OXO-1,3-DIHYDROBENZIMIDAZOL-1-YL)PIPERIDINE
Systematic Name English
R-30507
Code English
4-(2-OXO-1-BENZIMIDAZOLINYL)PIPERIDINE
Systematic Name English
1-(4-PIPERIDINYL)-2-BENZIMIDAZOLONE
Systematic Name English
2H-BENZIMIDAZOL-2-ONE, 1,3-DIHYDRO-1-(4-PIPERIDINYL)-
Systematic Name English
1-(PIPERIDIN-4-YL)-1,3-DIHYDRO-2H-BENZIMIDAZOL-2-ONE
Systematic Name English
PIMOZIDE IMPURITY A [EP IMPURITY]
Common Name English
4-(2-OXO-1-BENZIMIDAZOLY)PIPERIDINE
Systematic Name English
4-(2-OXO-1,3-DIHYDRO-2H-BENZIMIDAZOL-1-YL)PIPERIDINE
Systematic Name English
Code System Code Type Description
FDA UNII
4RP0AED2PC
Created by admin on Sat Dec 16 08:23:54 UTC 2023 , Edited by admin on Sat Dec 16 08:23:54 UTC 2023
PRIMARY
CAS
20662-53-7
Created by admin on Sat Dec 16 08:23:54 UTC 2023 , Edited by admin on Sat Dec 16 08:23:54 UTC 2023
PRIMARY
ECHA (EC/EINECS)
243-950-3
Created by admin on Sat Dec 16 08:23:54 UTC 2023 , Edited by admin on Sat Dec 16 08:23:54 UTC 2023
PRIMARY
EPA CompTox
DTXSID0057679
Created by admin on Sat Dec 16 08:23:54 UTC 2023 , Edited by admin on Sat Dec 16 08:23:54 UTC 2023
PRIMARY
PUBCHEM
88638
Created by admin on Sat Dec 16 08:23:54 UTC 2023 , Edited by admin on Sat Dec 16 08:23:54 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> METABOLITE
This metabolism is catalyzed mainly by the cytochrome P450 3A4 (CYP 3A4) enzymatic system and to a lesser extent, by cytochrome P450 1A2 (CYP 1A2) and cytochrome P450 2D6 (CYP 2D6)
MAJOR
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP