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2-(2,5-Hexadienyl)aniline, also known as 2-(2,5-Hexadienyl)phenylamine, is an organic compound with the chemical formula C12H15N. It is a derivative of aniline, where a 2,5-hexadienyl group replaces one hydrogen atom on the aniline molecule. 2-(2,5-hexadienyl)aniline is characterized by its conjugated double bond system, which extends from the hexadienyl group to the phenyl ring, providing it with unique chemical and physical properties. It is used as an intermediate in the synthesis of various dyes, pigments, and pharmaceuticals, and is known for its potential applications in the production of azo dyes due to its ability to form stable color compounds. The compound is typically synthesized through the reaction of aniline with 2,5-hexadienyl halides or through other organic synthesis routes. It is important to handle 2-(2,5-hexadienyl)aniline with care due to its potential reactivity and the need to adhere to safety protocols in chemical manufacturing and research settings.

76916-50-2

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76916-50-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76916-50-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,1 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 76916-50:
(7*7)+(6*6)+(5*9)+(4*1)+(3*6)+(2*5)+(1*0)=162
162 % 10 = 2
So 76916-50-2 is a valid CAS Registry Number.

76916-50-2Upstream product

76916-50-2Relevant academic research and scientific papers

Palladium-Assisted N-Alkylation of Indoles: Attempted Application to Polycyclization

Hegedus, Louis S.,Winton, Peter M.,Varaprath Sudarsanan

, p. 2215 - 2221 (2007/10/02)

The palladium(II) complexes of the olefins ethene, propene, and 1-hexene reacted with 1-lithioindole to produce N-alkylated indoles exclusively.Attempts to perform this N-alkylation intramoleculary (to form tricyclic material from 2-allylskatole) failed.Anilines with dienic side chains in the 2-position were subjected to Pd(II)-assisted cyclization conditions in attempts to induce polycyclization.However, only monocyclization was observed.

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