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Details

Stereochemistry RACEMIC
Molecular Formula C18H12Cl2N2O
Molecular Weight 343.207
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BECLICONAZOLE

SMILES

ClC1=CC2=C(OC(=C2)C(N3C=CN=C3)C4=C(Cl)C=CC=C4)C=C1

InChI

InChIKey=ZSTBJMFRJPALNV-UHFFFAOYSA-N
InChI=1S/C18H12Cl2N2O/c19-13-5-6-16-12(9-13)10-17(23-16)18(22-8-7-21-11-22)14-3-1-2-4-15(14)20/h1-11,18H

HIDE SMILES / InChI

Molecular Formula C18H12Cl2N2O
Molecular Weight 343.207
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

PubMed

PubMed

TitleDatePubMed
Gas chromatographic-mass spectrometric determination of two new antimycotic agents, 1-[(5-chloro-2-benzofuranyl)(2-chlorophenyl)methyl]-1H-imidazole and 1-[(5-bromo-2-benzofuranyl)phenylmethyl]-1H-imidazole, in rabbit plasma following topical administration: a preliminary comparison with bifonazole.
1991 Jun 14
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:03:22 GMT 2023
Edited
by admin
on Fri Dec 15 16:03:22 GMT 2023
Record UNII
5361814USE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BECLICONAZOLE
INN  
INN  
Official Name English
(±)-1-(O-CHLORO-.ALPHA.-(5-CHLORO-2-BENZOFURANYL)BENZYL)IMIDAZOLE
Common Name English
becliconazole [INN]
Common Name English
1H-IMIDAZOLE, 1-((5-CHLORO-2-BENZOFURANYL)(2-CHLOROPHENYL)METHYL)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C514
Created by admin on Fri Dec 15 16:03:22 GMT 2023 , Edited by admin on Fri Dec 15 16:03:22 GMT 2023
Code System Code Type Description
EVMPD
SUB05676MIG
Created by admin on Fri Dec 15 16:03:22 GMT 2023 , Edited by admin on Fri Dec 15 16:03:22 GMT 2023
PRIMARY
ChEMBL
CHEMBL2105923
Created by admin on Fri Dec 15 16:03:22 GMT 2023 , Edited by admin on Fri Dec 15 16:03:22 GMT 2023
PRIMARY
INN
6771
Created by admin on Fri Dec 15 16:03:22 GMT 2023 , Edited by admin on Fri Dec 15 16:03:22 GMT 2023
PRIMARY
PUBCHEM
65915
Created by admin on Fri Dec 15 16:03:22 GMT 2023 , Edited by admin on Fri Dec 15 16:03:22 GMT 2023
PRIMARY
CAS
112893-26-2
Created by admin on Fri Dec 15 16:03:22 GMT 2023 , Edited by admin on Fri Dec 15 16:03:22 GMT 2023
PRIMARY
FDA UNII
5361814USE
Created by admin on Fri Dec 15 16:03:22 GMT 2023 , Edited by admin on Fri Dec 15 16:03:22 GMT 2023
PRIMARY
EPA CompTox
DTXSID40869557
Created by admin on Fri Dec 15 16:03:22 GMT 2023 , Edited by admin on Fri Dec 15 16:03:22 GMT 2023
PRIMARY
SMS_ID
100000086092
Created by admin on Fri Dec 15 16:03:22 GMT 2023 , Edited by admin on Fri Dec 15 16:03:22 GMT 2023
PRIMARY
NCI_THESAURUS
C72954
Created by admin on Fri Dec 15 16:03:22 GMT 2023 , Edited by admin on Fri Dec 15 16:03:22 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY