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(E)-1-chloro-4-(4-chlorophenyl)-2-butene is an organic compound with the molecular formula C10H9Cl2. It is a conjugated diene, featuring a 1,3-butadiene backbone with a chlorine atom at the 1-position and a 4-chlorophenyl group at the 4-position. This molecule is characterized by its planar structure due to the conjugation of the double bonds and the phenyl ring. It is a colorless liquid with a pungent odor and is soluble in organic solvents. (E)-1-chloro-4-(4-chlorophenyl)-2-butene is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and insecticides. Due to its reactivity and the presence of two chlorine atoms, it can undergo a range of chemical reactions, including substitution, addition, and elimination reactions.

97163-33-2

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97163-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97163-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,1,6 and 3 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 97163-33:
(7*9)+(6*7)+(5*1)+(4*6)+(3*3)+(2*3)+(1*3)=152
152 % 10 = 2
So 97163-33-2 is a valid CAS Registry Number.

97163-33-2Relevant academic research and scientific papers

Synthesis and Class III Antiarrhythmic Activity of (Phenylbut-2-enyl)ammonium Salts. Effect of Conformation on Activity

Morgan, Thomas K.,Wohl, Ronald A.,Lumma, William C.,Wan, Chung-Nan,Davey, David D.,et al.

, p. 1398 - 1405 (2007/10/02)

The syntheses of seven 4-(substituted phenyl)but -2-en(or yn)yl quaternary ammonium salts and four related tertiary amines are described.The Meerwein arylation reaction was the preferred synthetic method for the required intermediate 1-aryl-4-halo-2-buten

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