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

Details

Stereochemistry ACHIRAL
Molecular Formula C7H4F3NO3
Molecular Weight 207.1068
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-TRIFLUOROMETHYL-4-NITROPHENOL

SMILES

OC1=CC=C(C(=C1)C(F)(F)F)[N+]([O-])=O

InChI

InChIKey=ZEFMBAFMCSYJOO-UHFFFAOYSA-N
InChI=1S/C7H4F3NO3/c8-7(9,10)5-3-4(12)1-2-6(5)11(13)14/h1-3,12H

HIDE SMILES / InChI

Molecular Formula C7H4F3NO3
Molecular Weight 207.1068
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Multi-residue determination of phenolic and salicylanilide anthelmintics and related compounds in bovine kidney by liquid chromatography-tandem mass spectrometry.
2009-11-13
Failure of ATP supply to match ATP demand: the mechanism of toxicity of the lampricide, 3-trifluoromethyl-4-nitrophenol (TFM), used to control sea lamprey (Petromyzon marinus) populations in the Great Lakes.
2009-10-04
Molecular interactions of pesticides at the soil-water interface.
2008-08-01
Prediction of lethal/effective concentration/dose in the presence of multiple auxiliary covariates and components of variance.
2007-09
Residues of the lampricides 3-trifluoromethyl-4-nitrophenol and niclosamide in muscle tissue of rainbow trout.
2005-06-29
Relatively rapid loss of lampricide residues from fillet tissue of fish after routine treatment.
2002-11-06
Rapid loss of lampricide from catfish and rainbow trout following routine treatment.
2002-11-06
Determination of 3-trifluoromethyl-4-nitrophenol and 3-trifluoromethyl-4-nitrophenol glucuronide in edible fillet tissue of rainbow trout and channel catfish by solid-phase extraction and liquid chromatography.
2001-04-28
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:06:35 GMT 2025
Edited
by admin
on Mon Mar 31 19:06:35 GMT 2025
Record UNII
96W52A3IFS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-TRIFLUOROMETHYL-4-NITROPHENOL
Systematic Name English
TFM
MI  
Preferred Name English
LAMPRECID
Brand Name English
HOE-2770
Code English
4-NITRO-3-TRIFLUOROMETHYLPHENOL
Common Name English
NSC-59758
Code English
TRIFLUOROMETHYL-4-NITROPHENOL, 3-
Systematic Name English
4-NITRO-3-(TRIFLUOROMETHYL)PHENOL
Systematic Name English
TFM [MI]
Common Name English
4-NITRO-3-TRIFLUOROMETHYLPHENOL [HSDB]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 36201
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
Code System Code Type Description
CAS
88-30-2
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-818-2
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
PRIMARY
NSC
59758
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
PRIMARY
HSDB
7506
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
PRIMARY
EPA CompTox
DTXSID7021788
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
PRIMARY
WIKIPEDIA
TFM (piscicide)
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
PRIMARY
FDA UNII
96W52A3IFS
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
PRIMARY
MESH
C003687
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
PRIMARY
MERCK INDEX
m10671
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
PRIMARY Merck Index
PUBCHEM
6931
Created by admin on Mon Mar 31 19:06:35 GMT 2025 , Edited by admin on Mon Mar 31 19:06:35 GMT 2025
PRIMARY