U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C12H4Cl2F6N4OS
Molecular Weight 437.148
Optical Activity ( - )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FIPRONIL, (R)-

SMILES

NC1=C([S@@+]([O-])C(F)(F)F)C(=NN1C2=C(Cl)C=C(C=C2Cl)C(F)(F)F)C#N

InChI

InChIKey=ZOCSXAVNDGMNBV-AREMUKBSSA-N
InChI=1S/C12H4Cl2F6N4OS/c13-5-1-4(11(15,16)17)2-6(14)8(5)24-10(22)9(7(3-21)23-24)26(25)12(18,19)20/h1-2H,22H2/t26-/m1/s1

HIDE SMILES / InChI

Molecular Formula C12H4Cl2F6N4OS
Molecular Weight 437.148
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 13:40:19 UTC 2023
Edited
by admin
on Sat Dec 16 13:40:19 UTC 2023
Record UNII
95Q7F5498G
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FIPRONIL, (R)-
Common Name English
1H-PYRAZOLE-3-CARBONITRILE, 5-AMINO-1-(2,6-DICHLORO-4-(TRIFLUOROMETHYL)PHENYL)-4-((R)-(TRIFLUOROMETHYL)SULFINYL)-
Systematic Name English
R-(-)-FIPRONIL
Common Name English
(-)-FIPRONIL
Common Name English
5-AMINO-1-(2,6-DICHLORO-4-(TRIFLUOROMETHYL)PHENYL)-4-((R)-(TRIFLUOROMETHYL)SULFINYL)-1H-PYRAZOLE-3-CARBONITRILE
Systematic Name English
(R)-FIPRONIL
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID801019547
Created by admin on Sat Dec 16 13:40:19 UTC 2023 , Edited by admin on Sat Dec 16 13:40:19 UTC 2023
PRIMARY
PUBCHEM
15278226
Created by admin on Sat Dec 16 13:40:19 UTC 2023 , Edited by admin on Sat Dec 16 13:40:19 UTC 2023
PRIMARY
CHEBI
83395
Created by admin on Sat Dec 16 13:40:19 UTC 2023 , Edited by admin on Sat Dec 16 13:40:19 UTC 2023
PRIMARY
CAS
302578-97-8
Created by admin on Sat Dec 16 13:40:19 UTC 2023 , Edited by admin on Sat Dec 16 13:40:19 UTC 2023
PRIMARY
FDA UNII
95Q7F5498G
Created by admin on Sat Dec 16 13:40:19 UTC 2023 , Edited by admin on Sat Dec 16 13:40:19 UTC 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
ENANTIOMER -> ENANTIOMER