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3-anilino-2-phenyl-acrylonitrile is an organic compound characterized by its molecular formula C15H12N2. It is a derivative of acrylonitrile, featuring an aniline group attached to the 3-position and a phenyl group at the 2-position. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and dyes due to its reactive nitrile and aniline groups. The compound is also of interest in materials science for its possible use in the development of polymers with specific properties. Its structure allows for a range of chemical reactions, making it a versatile building block in organic synthesis.

1215-26-5

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1215-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1215-26-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1215-26:
(6*1)+(5*2)+(4*1)+(3*5)+(2*2)+(1*6)=45
45 % 10 = 5
So 1215-26-5 is a valid CAS Registry Number.

1215-26-5Relevant academic research and scientific papers

Enaminonitriles in heterocyclic synthesis: Novel synthesis of 3-aminopyrroles and pyrrolo[3,2-d] pyrimidine derivatives

Salaheldin, Abdellatif M.

experimental part, p. 564 - 570 (2009/02/03)

Several new 3-aminopyrrole derivatives have been synthesized from 3-substituted amino-2-phenylacrylonitriles using Thorpe-Ziegler cyclization. These substituted pyrroles are readily converted into 5H-pyrrolo[3,2-d] pyrimidines (9-deazapurines).

Addition of diazoacetonitrile to N-benzylidene-anilines. Synthesis and decomposition of 4-cyano-1,5-diaryl,Δ2-1,2,3-triazolines

Roelants,Bruylants

, p. 2229 - 2232 (2007/10/06)

Addition of diazoacetonitrile to para-substituted N-benzilidene-anilines has been studied. The addition is easier if the substituent is an electrodonating group. Products obtained are Δ2-1,2,3-triazolines or aziridnes, and enamines resulting from the decomposition of the triazolines with migration of the 5-aryl substituent. Decomposition of the triazolines under various conditions has also been studied.

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