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197017

Sigma-Aldrich

4-Chloro-3,5-dinitrobenzotrifluoride

98%

Synonym(s):

CDNT, DNT-Cl

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About This Item

Linear Formula:
ClC6H2(NO2)2CF3
CAS Number:
393-75-9
Molecular Weight:
270.55
Beilstein:
1220937
EC Number:
206-889-3
MDL number:
MFCD00007068
UNSPSC Code:
12352100
PubChem Substance ID:
24851818
NACRES:
NA.22

Assay

98%

form

solid

mp

50-55 °C (lit.)

solubility

water: insoluble

functional group

chloro

SMILES string

[O-][N+](=O)c1cc(cc(c1Cl)[N+]([O-])=O)C(F)(F)F

InChI

1S/C7H2ClF3N2O4/c8-6-4(12(14)15)1-3(7(9,10)11)2-5(6)13(16)17/h1-2H

InChI key

HFHAVERNVFNSHL-UHFFFAOYSA-N

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Application

4-Chloro-3,5-dinitrobenzotrifluoride was used:
  • as derivatization reagent in determination of amikacin in water samples and amino acids by HPLC
  • in the synthesis of N-(2,6-dinitro-4-trifluoromethylphenyl)aniline derivatives
  • in the synthesis of 4,6-dinitro-2,8-bis(trifluoromethyl)phenothiazine and isopropyl-2,6-dinitro-4-trifluoromethylphenyl sulfide

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H302,H310,H315,H319

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

258.8 °F - closed cup

Flash Point(C)

126 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCK0448
MKBV2179V
03904LH
04310CL
0424CJ

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K A Werbovetz et al.
Molecular and biochemical parasitology, 98(1), 53-65 (1999-02-24)
Past work suggests that tubulin from kinetoplastid parasites may present an excellent drug target. To explore this possibility, tubulin was purified on a milligram scale from Leishmania mexicana amazonensis promastigotes by sonication, DEAE-Sepharose chromatography, and one cycle of assembly-disassembly. Purified
Tianyu Shi et al.
Analytica chimica acta, 654(2), 154-161 (2009-10-27)
This work presents an high-performance liquid chromatography method for the determination of amino acids after precolumn derivatization with 4-chloro-3,5-dinitrobenzotrifluoride (CNBF) which can readily react with both primary and secondary amines. The precolumn derivatization conditions, including the CNBF concentration, reaction pH
C Guastadisegni et al.
Ecotoxicology and environmental safety, 17(1), 21-29 (1989-02-01)
3,5-Dinitro-4-chloro-alpha,alpha,alpha-trifluorotoluene (DNCTT) is an intermediate in the synthesis of dinitroaniline herbicides and was involved in an episode of ground water pollution in 1977. The compound presents a high environmental persistence, which may have possible implications concerning public health. In one
In vitro effects of substituted toluenes on mitochondria isolated from rat liver.
C M Schiller
Biochemical pharmacology, 29(18), 2485-2489 (1980-09-15)
DERIVATIVES OF 4-CHLORO-3, 5-DINITROBENZOTRIFLUORIDE V. SYNTHESIS OF 4, 6-DINITRO-2, 8-BIS (TRIFLUOROMETHYL) PHENOTHIAZINE (1), ISOPROPYL 2, 6-DINITRO-4-TRIFLUOROMETHYLPHENYL SULFIDE (2) AND BIS (2, 6-DINITRO-4-TRIFLUOROMETHYLPHENYL) DISULFIDE (3).
D' aamico JJ, et al.
Phosphorus, Sulfur, and Silicon and the Related Elements, 7(2), 143-148 (1979)
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