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"Benzenamine, N-(4-methylphenyl)-2-nitro-4-(trifluoromethyl)-" is a complex organic chemical compound with the molecular formula C15H12F3N3O2. It is a derivative of benzenamine, also known as aniline, which is a primary aromatic amine. Benzenamine, N-(4-methylphenyl)-2-nitro-4-(trifluoromethyl)- features a 4-methylphenyl group attached to the nitrogen atom, a 2-nitro group, and a 4-trifluoromethyl group on the benzene ring. It is a yellow crystalline solid with potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound's properties, such as its melting point, solubility, and toxicity, are important considerations for its safe handling and use in various chemical processes.

1598-33-0

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1598-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1598-33-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,9 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1598-33:
(6*1)+(5*5)+(4*9)+(3*8)+(2*3)+(1*3)=100
100 % 10 = 0
So 1598-33-0 is a valid CAS Registry Number.

1598-33-0Relevant academic research and scientific papers

Continuous-flow synthesis of 1-substituted benzotriazoles from chloronitrobenzenes and amines in a C-N bond formation/hydrogenation/ diazotization/cyclization sequence

Chen, Mao,Buchwald, Stephen L.

supporting information, p. 4247 - 4250 (2013/05/08)

Two approaches have been developed for the regiospecific continuous-flow synthesis of 1-substituted benzotriazoles. They begin with either an S NAr reaction at high temperature or Pd catalysis and involve consecutive multiphase processes, allow

A practical oxone - Mediated, high-throughput, solution-phase synthesis of benzimidazoles from 1,2-phenylenediamines and aldehydes and its application to preparative scale synthesis

Beaulieu, Pierre L.,Hache, Bruno,Von Moos, Elisabeth

, p. 1683 - 1692 (2007/10/03)

Addition of oxone to a mixture of a 1,2-phenylenediamine and an aldehyde in wet DMF at room temperature results in rapid formation of benzimidazoles under very mild conditions. The reaction is applicable to a wide range of substrates including aliphatic,

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