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Details

Stereochemistry RACEMIC
Molecular Formula C16H13Cl3N2OS
Molecular Weight 387.711
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TIOCONAZOLE

SMILES

ClC1=C(COC(CN2C=CN=C2)C3=CC=C(Cl)C=C3Cl)C=CS1

InChI

InChIKey=QXHHHPZILQDDPS-UHFFFAOYSA-N
InChI=1S/C16H13Cl3N2OS/c17-12-1-2-13(14(18)7-12)15(8-21-5-4-20-10-21)22-9-11-3-6-23-16(11)19/h1-7,10,15H,8-9H2

HIDE SMILES / InChI

Molecular Formula C16H13Cl3N2OS
Molecular Weight 387.711
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:34:31 UTC 2023
Edited
by admin
on Fri Dec 15 18:34:31 UTC 2023
Record UNII
S57Y5X1117
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TIOCONAZOLE
EP   INCI   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN   INN   INCI  
Official Name English
TIOCONAZOLE [ORANGE BOOK]
Common Name English
VAGISTAT-1
Brand Name English
TIOCONAZOLE [VANDF]
Common Name English
TIOCONAZOLE [JAN]
Common Name English
NSC-759169
Code English
tioconazole [INN]
Common Name English
Tioconazole [WHO-DD]
Common Name English
TIOCONAZOLE [USAN]
Common Name English
UK-20,349
Code English
TIOCONAZOLE [MI]
Common Name English
TIOCONAZOLE [MART.]
Common Name English
TIOCONAZOLE [EP MONOGRAPH]
Common Name English
VAGISTAT
Brand Name English
UK-20349
Code English
TIOCONAZOLE [USP-RS]
Common Name English
TIOCONAZOLE [USP IMPURITY]
Common Name English
TIOCONAZOLE [INCI]
Common Name English
TIOCONAZOLE [USP MONOGRAPH]
Common Name English
1H-IMIDAZOLE, 1-(2-((2-CHLORO-3-THIENYL)METHOXY)-2-(2,4-DICHLOROPHENYL)ETHYL)-
Systematic Name English
Classification Tree Code System Code
NDF-RT N0000008217
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
NCI_THESAURUS C514
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
WHO-VATC QD01AC07
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
WHO-ATC G01AF08
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
NDF-RT N0000175487
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
WHO-ATC D01AC07
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
WHO-VATC QG01AF08
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
Code System Code Type Description
MERCK INDEX
m10878
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY Merck Index
RXCUI
38298
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY RxNorm
CHEBI
9604
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
LACTMED
Tioconazole
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
EVMPD
SUB11080MIG
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
DRUG BANK
DB01007
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
SMS_ID
100000077210
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
DRUG CENTRAL
2675
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
CAS
65899-73-2
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
WIKIPEDIA
TIOCONAZOLE
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
ECHA (EC/EINECS)
265-973-8
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
EPA CompTox
DTXSID3046619
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
DAILYMED
S57Y5X1117
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
FDA UNII
S57Y5X1117
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
NSC
759169
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
INN
4572
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
MESH
C020527
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
PUBCHEM
5482
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
RS_ITEM_NUM
1667439
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
NCI_THESAURUS
C29500
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
ChEMBL
CHEMBL1200438
Created by admin on Fri Dec 15 18:34:31 UTC 2023 , Edited by admin on Fri Dec 15 18:34:31 UTC 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
Related Record Type Details
IMPURITY -> PARENT
correction factors: for the calculation of contents, multiply the peak areas of the following impurities by the corresponding correction factor: impurity C = 1.7
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
ACTIVE MOIETY