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(Z)-3-bromo-2,3-diphenylprop-2-enenitrile is an organic compound characterized by its molecular formula C15H11BrN. It is a derivative of prop-2-enenitrile, featuring a bromine atom at the 3rd carbon position and two phenyl groups attached to the 2nd and 3rd carbons. The "Z" configuration indicates that the bromine and phenyl groups are on the same side of the double bond, which is crucial for its stereochemistry. (Z)-3-bromo-2,3-diphenylprop-2-enenitrile is known for its potential applications in the synthesis of various pharmaceuticals and organic materials due to its unique structure and reactivity. It is typically synthesized through various organic reactions and is used as an intermediate in the preparation of more complex molecules.

1824-02-8

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1824-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1824-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1824-02:
(6*1)+(5*8)+(4*2)+(3*4)+(2*0)+(1*2)=68
68 % 10 = 8
So 1824-02-8 is a valid CAS Registry Number.

1824-02-8Relevant academic research and scientific papers

Gallium (iii)-catalysed bromocyanation of alkynes: Regio- and stereoselective synthesis of β-bromo-α,β-unsaturated nitriles

Murai, Masahito,Hatano, Ryo,Kitabata, Sachie,Ohe, Kouichi

supporting information; experimental part, p. 2375 - 2377 (2011/04/18)

Treatment of arylacetylenes and cyanogen bromide in ClCH2CH 2Cl with a catalytic amount of GaCl3 afforded (Z)-β-bromoacrylonitriles with high regio- and stereoselectivity.

Some Properties of Cyclopropenone Oximes under Beckmann Reaction Conditions

Yoshida, Hiroshi,Yoshida, Keisuke,Totani, Hiroyuki,Ogata, Tsuyoshi,Matsumoto, Kiyoshi

, p. 3579 - 3582 (2007/10/02)

The reaction of diphenylcyclopropenone oxime (1a) with acetyl or tosyl isocyanate, carboxylic anhydrides, or nitrohalobenzenes yielded the cyclopropenone O-substituted oxime derivatives.Treating with thionyl bromide and chloride 1a gave 3-haloacrylonitriles.Whereas 1a as well as other cyclopropenone oximes, were stable under acidic conditions, heating in methanolic sodium hydroxide gave the ring-opened α,α-dimethoxyketones oximes.

Derivatives of the 1,2-diarylethylene- and pharmaceutical compositions thereof

-

, (2008/06/13)

The invention relates to derivatives of 1,2-diarylethylene and to a process for their preparation. The compounds have valuable pharmaceutical properties and may be used as medicaments.

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