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Details

Stereochemistry RACEMIC
Molecular Formula C19H17Cl3N2S.HNO3
Molecular Weight 474.789
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BUTOCONAZOLE NITRATE

SMILES

O[N+]([O-])=O.ClC1=CC=C(CCC(CN2C=CN=C2)SC3=C(Cl)C=CC=C3Cl)C=C1

InChI

InChIKey=ZHPWRQIPPNZNML-UHFFFAOYSA-N
InChI=1S/C19H17Cl3N2S.HNO3/c20-15-7-4-14(5-8-15)6-9-16(12-24-11-10-23-13-24)25-19-17(21)2-1-3-18(19)22;2-1(3)4/h1-5,7-8,10-11,13,16H,6,9,12H2;(H,2,3,4)

HIDE SMILES / InChI

Molecular Formula HNO3
Molecular Weight 63.0128
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C19H17Cl3N2S
Molecular Weight 411.776
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 18:59:53 UTC 2023
Edited
by admin
on Fri Dec 15 18:59:53 UTC 2023
Record UNII
4805237NP5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BUTOCONAZOLE NITRATE
MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN  
Official Name English
BUTOCONAZOLE NITRATE [MI]
Common Name English
BUTOCONAZOLE NITRATE [USP-RS]
Common Name English
RS-35887
Code English
BUTOCONAZOLE NITRATE [ORANGE BOOK]
Common Name English
BUTOCONAZOLE NITRATE [VANDF]
Common Name English
BUTOCONAZOLE NITRATE [USAN]
Common Name English
Butoconazole nitrate [WHO-DD]
Common Name English
1H-IMIDAZOLE, 1-(4-(4-CHLOROPHENYL)-2-((2,6-DICHLOROPHENYL)THIO)BUTYL)-, MONONITRATE, (±)-
Systematic Name English
BUTOCONAZOLE NITRATE [USP MONOGRAPH]
Common Name English
BUTOCONAZOLE NITRATE [MART.]
Common Name English
(±)-1-(4-(P-CHLOROPHENYL)-2-((2,6-DICHLOROPHENYL)THIO)BUTYL)IMIDAZOLE MONONITRATE
Common Name English
GYNAZOLE
Brand Name English
FEMSTAT
Brand Name English
RS-35887-00-10-3
Code English
Classification Tree Code System Code
NCI_THESAURUS C514
Created by admin on Fri Dec 15 18:59:54 UTC 2023 , Edited by admin on Fri Dec 15 18:59:54 UTC 2023
Code System Code Type Description
CAS
64872-77-1
Created by admin on Fri Dec 15 18:59:53 UTC 2023 , Edited by admin on Fri Dec 15 18:59:53 UTC 2023
PRIMARY
ChEMBL
CHEMBL1295
Created by admin on Fri Dec 15 18:59:53 UTC 2023 , Edited by admin on Fri Dec 15 18:59:53 UTC 2023
PRIMARY
PUBCHEM
47471
Created by admin on Fri Dec 15 18:59:54 UTC 2023 , Edited by admin on Fri Dec 15 18:59:54 UTC 2023
PRIMARY
NCI_THESAURUS
C47427
Created by admin on Fri Dec 15 18:59:54 UTC 2023 , Edited by admin on Fri Dec 15 18:59:54 UTC 2023
PRIMARY
RXCUI
47464
Created by admin on Fri Dec 15 18:59:54 UTC 2023 , Edited by admin on Fri Dec 15 18:59:54 UTC 2023
PRIMARY RxNorm
DRUG BANK
DB00639
Created by admin on Fri Dec 15 18:59:53 UTC 2023 , Edited by admin on Fri Dec 15 18:59:53 UTC 2023
PRIMARY
EPA CompTox
DTXSID6045452
Created by admin on Fri Dec 15 18:59:53 UTC 2023 , Edited by admin on Fri Dec 15 18:59:53 UTC 2023
PRIMARY
SMS_ID
100000084860
Created by admin on Fri Dec 15 18:59:54 UTC 2023 , Edited by admin on Fri Dec 15 18:59:54 UTC 2023
PRIMARY
FDA UNII
4805237NP5
Created by admin on Fri Dec 15 18:59:53 UTC 2023 , Edited by admin on Fri Dec 15 18:59:53 UTC 2023
PRIMARY
DAILYMED
4805237NP5
Created by admin on Fri Dec 15 18:59:53 UTC 2023 , Edited by admin on Fri Dec 15 18:59:53 UTC 2023
PRIMARY
RS_ITEM_NUM
1082300
Created by admin on Fri Dec 15 18:59:54 UTC 2023 , Edited by admin on Fri Dec 15 18:59:54 UTC 2023
PRIMARY
MERCK INDEX
m2801
Created by admin on Fri Dec 15 18:59:53 UTC 2023 , Edited by admin on Fri Dec 15 18:59:53 UTC 2023
PRIMARY Merck Index
CHEBI
3241
Created by admin on Fri Dec 15 18:59:53 UTC 2023 , Edited by admin on Fri Dec 15 18:59:53 UTC 2023
PRIMARY
EVMPD
SUB00918MIG
Created by admin on Fri Dec 15 18:59:53 UTC 2023 , Edited by admin on Fri Dec 15 18:59:53 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY