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Benzamide, N-(4-phenyl-3-butenyl)-, (E)- is an organic compound with the chemical formula C15H15NO. It is a derivative of benzamide, featuring a 4-phenyl-3-butenyl group attached to the nitrogen atom. Benzamide, N-(4-phenyl-3-butenyl)-, (E)- is characterized by its (E)-configuration, indicating the geometric arrangement of the double bond in the 3-butenyl chain. It is a white to off-white crystalline solid and is used in various chemical and pharmaceutical applications, such as the synthesis of pharmaceuticals and as an intermediate in organic synthesis. Due to its specific structure, it may exhibit unique chemical properties and reactivity compared to other benzamide derivatives.

7651-77-6

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7651-77-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7651-77-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,5 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7651-77:
(6*7)+(5*6)+(4*5)+(3*1)+(2*7)+(1*7)=116
116 % 10 = 6
So 7651-77-6 is a valid CAS Registry Number.

7651-77-6Downstream Products

7651-77-6Relevant academic research and scientific papers

Direct Coupling between β-Functionalized Organolithium Compounds and Aryl and Vinyl Halides

Barluenga, Jose,Montserrat, Javier M.,Florez, Josefa

, p. 6183 - 6186 (1992)

Treatment of N-lithio-N-(2-lithioethyl)benzamide with different aromatic and vinylic halides affords directly the corresponding substitution products: functionalized benzamides 3-10.

Direct Coupling of Functionalized Organolithium Compounds with Aryl and Vinyl Halides

Barluenga, Jose,Montserrat, Javier M.,Florez, Josefa

, p. 5976 - 5980 (2007/10/02)

The reaction between β- and γ-nitrogen-functionalized and γ- and ε-oxygen-functionalized organolithium compounds 3, 4, 30-32 and different aromatic, heteroaromatic, and vinylic halides affords directly the corresponding substitution products: functionalized benzamides 5-26 and alcohols 33-37.Symmetrical and mixed products of double coupling 38-40 were also prepared from 1,4-diiodobenzene.The formation of alkyl halides as intermediates has been verified.Aryl or vinyl halides giving rise to unstable aryl or vinyllithium reagents were unsuccessful in the coupling reaction.

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