1429194-04-6 Usage
Description
N,N-Bis(4-bromophenyl)-4-fluoroaniline is a chemical compound characterized by the molecular formula C18H13Br2FN. It is a substituted aniline derivative featuring two 4-bromophenyl groups and a 4-fluoro group attached to the nitrogen atom. This versatile compound is recognized for its utility in organic synthesis and pharmaceutical research, where it serves as a fundamental building block for the creation of more complex molecular structures. Its applications extend across various industries, including pharmaceuticals, agrochemicals, and materials science, making it a valuable intermediate in the production of dyes, pigments, and other organic compounds. However, due to potential health and environmental risks, careful handling and storage are imperative.
Uses
Used in Organic Synthesis:
N,N-Bis(4-bromophenyl)-4-fluoroaniline is utilized as a key building block in organic synthesis for the development of complex molecules. Its unique structure allows for the formation of various chemical entities, contributing to the advancement of chemical research and innovation.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N,N-Bis(4-bromophenyl)-4-fluoroaniline is employed as an intermediate in the synthesis of new drug candidates. Its presence in the molecular structure can influence the pharmacological properties of the final product, making it a valuable component in drug discovery and development.
Used in Dye and Pigment Production:
N,N-Bis(4-bromophenyl)-4-fluoroaniline is used as an intermediate in the production of dyes and pigments. Its chemical properties enable the creation of a wide range of colorants used in various applications, from textiles to printing inks.
Used in Agrochemicals:
In the agrochemical sector, N,N-Bis(4-bromophenyl)-4-fluoroaniline is leveraged for the synthesis of active ingredients in pesticides and other agricultural chemicals. Its role in these products is crucial for enhancing crop protection and yield.
Used in Materials Science:
N,N-Bis(4-bromophenyl)-4-fluoroaniline contributes to the field of materials science by serving as a component in the development of new materials with specific properties. Its integration into material formulations can lead to advancements in areas such as polymer science and nanotechnology.
Check Digit Verification of cas no
The CAS Registry Mumber 1429194-04-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,1,9 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1429194-04:
(9*1)+(8*4)+(7*2)+(6*9)+(5*1)+(4*9)+(3*4)+(2*0)+(1*4)=166
166 % 10 = 6
So 1429194-04-6 is a valid CAS Registry Number.
1429194-04-6Relevant articles and documents
Construction of electrocatalytic electrodes bearing the triphenylamine nucleus covalently bound to carbon. A halogen dance in protonated aminotriphenylamines
Mayers, Brian T.,Fry, Albert J.
, p. 411 - 414 (2007/10/03)
The triarylamine nucleus has been attached to a carbon fiber electrode by diazotization of an aminotriphenylamine followed by electrochemical reduction. The resulting electrodes can electrocatalyze the oxidation of organic substrates. In acid, 4-amino-4′,4″-dibromotriphenylamine undergoes dismutation into a mixture of amines containing from 0 to 3 bromine atoms.
