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2,4-dinitro-N-[3-(trifluoromethyl)phenyl]aniline is a chemical compound with the molecular formula C13H8F3N3O4. It is an organic compound that belongs to the class of aniline derivatives, characterized by the presence of an amino group (-NH2) attached to a phenyl ring. This specific compound features two nitro groups (-NO2) at the 2nd and 4th positions of the phenyl ring, and a trifluoromethyl group (-CF3) at the 3rd position. The compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of dyes and pigments. Due to its complex structure and functional groups, it is important to handle 2,4-dinitro-N-[3-(trifluoromethyl)phenyl]aniline with care, as it may exhibit hazardous properties and require specific safety measures during its use and storage.

1869-67-6

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1869-67-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1869-67-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1869-67:
(6*1)+(5*8)+(4*6)+(3*9)+(2*6)+(1*7)=116
116 % 10 = 6
So 1869-67-6 is a valid CAS Registry Number.

1869-67-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-Dinitro-N-[3-(trifluoromethyl)phenyl]aniline

1.2 Other means of identification

Product number -
Other names UPCMLD0ENAT0518-4949:001

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1869-67-6 SDS

1869-67-6Downstream Products

1869-67-6Relevant academic research and scientific papers

Efficient synthetic route to aromatic secondary amines: Via Pd/RuPhos/TBAB-catalyzed cross coupling

Gaur, Pinki,Durga Bhaskar Yamajala,Banerjee, Shaibal

, p. 6523 - 6529 (2017/07/17)

Herein, C-N cross coupling methodology was developed for the synthesis of a diverse range of nitro-substituted secondary amines. A variety of strained, aliphatic, and aromatic precursors were effectively used, with low catalyst and ligand loading ratios resulting in product formation in good yield. This method can act as an alternative to nucleophilic addition reactions. To cross couple electron-donating, electron-withdrawing, neutral, and aliphatic primary amines with alkyl/aryl halides, a combination of RuPhos and TBAB was carefully tuned. Further, characterization of these molecules was carried out using FT-IR, 1H-NMR, 13C-NMR, 19F-NMR, single crystal XRD, and C, H, and N elemental analyses.

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