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4'-Aminobiphenyl-4-carbonitrile, a chemical compound with the molecular formula C13H10N2, is a derivative of biphenyl that features a cyanide group at the 4th carbon and an amino group at the 4' position. 4'-Aminobiphenyl-4-carbonitrile plays a significant role in organic synthesis and chemical research, serving as a building block for the creation of various pharmaceuticals and agrochemicals. Additionally, it is utilized as an intermediate in the production of dyes and pigments. Due to its potential hazards, special care must be taken during its handling and storage.

4854-84-6

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4854-84-6 Usage

Uses

Used in Organic Synthesis:
4'-Aminobiphenyl-4-carbonitrile is used as a building block in organic synthesis for the development of various pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a wide range of compounds with diverse applications in these industries.
Used in Chemical Research:
In the field of chemical research, 4'-Aminobiphenyl-4-carbonitrile serves as an important intermediate, contributing to the advancement of scientific knowledge and the discovery of new chemical reactions and processes.
Used in Dye and Pigment Production:
4'-Aminobiphenyl-4-carbonitrile is utilized as an intermediate in the production of dyes and pigments, playing a crucial role in the creation of colorants for various applications, including textiles, plastics, and printing inks.
Used in Pharmaceutical Industry:
4'-Aminobiphenyl-4-carbonitrile is used as a key component in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapies for various medical conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 4'-Aminobiphenyl-4-carbonitrile is employed as a building block for the synthesis of agrochemicals, such as pesticides and herbicides, which are essential for crop protection and agricultural productivity.
Precautions:
Due to the potential hazards associated with 4'-Aminobiphenyl-4-carbonitrile, it is essential to follow proper handling and storage procedures to minimize risks. This includes using appropriate personal protective equipment, ensuring proper ventilation, and storing the compound in a secure and well-marked container.

Check Digit Verification of cas no

The CAS Registry Mumber 4854-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,5 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4854-84:
(6*4)+(5*8)+(4*5)+(3*4)+(2*8)+(1*4)=116
116 % 10 = 6
So 4854-84-6 is a valid CAS Registry Number.

4854-84-6Relevant academic research and scientific papers

Novel and unexpected deamination during the palladium-catalysed cross- coupling of haloanilines and arylboronic acids

Hird, Michael,Seed, Alexander J.,Toyne, Kenneth J.

, p. 438 - 440 (2007/10/03)

Palladium-catalysed cross-coupling reactions involving haloanilines and arylboronic acids produce the expected biaryl products, but additionally a substantial quantity of the corresponding deaminated biaryl is also generated which constitutes a novel synthetic methodology.

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