ChemicalBook--->CAS DataBase List--->35375-74-7

35375-74-7

35375-74-7 Structure

35375-74-7 Structure
IdentificationBack Directory
[Name]

4-AMINO-2-CHLORO-5-NITROBENZOTRIFLUORIDE
[CAS]

35375-74-7
[Synonyms]

4-AMINO-2-CHLORO-5-NITROBENZOTRIFLUORIDE
5-chloro-2-nitro-5-trifluoromethylaniline
5-CHLORO-2-NITRO-4-(TRIFLUOROMETHYL)ANILINE
3-Chloro-6-nitro-4-(trifluoromethyl)Aniline
4-Amino-2-chloro-5-nitrobenzotrifluoride 97%
5-chloro-2-nitro-4-trifluoroMethyl-phenylaMine
5-Chloro-2-nitro-4-(trifluoromethyl)benzenamine
5-chloro-4-(trifluoromethyl)-2-nitrobenzenamine
Benzenamine, 5-chloro-2-nitro-4-(trifluoromethyl)-
5-Chloro-2-nitro-4-(trifluoromethyl)aniline, 2-Amino-4-chloro-5-(trifluoromethyl)nitrobenzene
[Molecular Formula]

C7H4ClF3N2O2
[MDL Number]

MFCD03788547
[MOL File]

35375-74-7.mol
[Molecular Weight]

240.57
Questions And AnswerBack Directory
[Synthesis]

We used 5-chloro-2-nitroaniline as a starting material and obtained the intermediate 4-AMINO-2-CHLORO-5-NITROBENZOTRIFLUORIDE in a relatively high yield through a four-step reaction involving iodination, acetylation protection, trifluoromethylation, and deacetylation. Through continuous experimentation, the yield of the trifluoromethylation step was found to be as high as 78%. The synthesis of 4-AMINO-2-CHLORO-5-NITROBENZOTRIFLUORIDE mainly involves four steps: iodination, acetylation protection, trifluoromethylation, and deacetylation. The synthetic route is shown in Figure 1.

Synthesis of 35375-74-7

Synthetic Route of 5-Chloro-2-nitro-4-(trifluoromethyl)aniline

Using 5-chloro-2-nitroaniline and elemental iodine as raw materials, the pesticide intermediate 4-AMINO-2-CHLORO-5-NITROBENZOTRIFLUORIDE is synthesized through a four-step reaction involving iodination, acetylation protection, trifluoromethylation, and deacetylation. This method has the following outstanding features: ① The raw materials are inexpensive and readily available; ② The reaction conditions are mild and easy to control; ③ The reaction system is simple, and the intermediate is easy to separate and purify; ④ The single-step yield is high, and the overall yield is moderate, showing potential development and application value.

Chemical PropertiesBack Directory
[Melting point ]

113 °C
[Boiling point ]

310.7±42.0 °C(Predicted)
[density ]

1.614±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

-3.78±0.25(Predicted)
[Appearance]

Light brown to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

26-36/37/39
[RIDADR ]

UN2811
[Hazard Note ]

Irritant
[HazardClass ]

6.1
[HS Code ]

2826199090
Hazard InformationBack Directory
[Uses]

5-Chloro-2-nitro-4-(trifluoromethyl)aniline is a reagent used in the preparation of fused imidazole biocides.
Spectrum DetailBack Directory
[Spectrum Detail]

4-AMINO-2-CHLORO-5-NITROBENZOTRIFLUORIDE(35375-74-7)1HNMR
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