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(Z)-2,4-dichloro-1-(2-phenylethenyl)-benzene, also known as β-chloro-α,α-dichlorostyrene, is an organic compound with the chemical formula C14H10Cl2. It is a colorless to pale yellow liquid with a molecular weight of 251.14 g/mol. (Z)-2,4-dichloro-1-(2-phenylethenyl)-benzene is characterized by the presence of two chlorine atoms at the 2nd and 4th positions of the benzene ring, and a phenylethenyl group (a phenyl ring with a vinyl group attached) at the 1st position. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is important to handle (Z)-2,4-dichloro-1-(2-phenylethenyl)-benzene with care, following proper safety protocols.

1657-69-8

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1657-69-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1657-69-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1657-69:
(6*1)+(5*6)+(4*5)+(3*7)+(2*6)+(1*9)=98
98 % 10 = 8
So 1657-69-8 is a valid CAS Registry Number.

1657-69-8Upstream product

1657-69-8Downstream Products

1657-69-8Relevant academic research and scientific papers

Synthesis and biological evaluation of 1,1-dichloro-2,3-diarylcyclopropanes as antitubulin and anti-breast cancer agents

Jonnalagadda, Sastry S.,Ter Haar, Ernst,Hamel, Ernest,Lin, Chii M.,Magarian, Robert A.,Day, Billy W.

, p. 715 - 722 (1997)

Z-1,1-Dichloro-2,3-diphenylcyclopropane (1) is an effective anti-breast cancer agent in rodents and in cell culture. We recently determined that 1 inhibits tubulin assembly in vitro, and causes microtubule loss in breast cancer cells, leading to accumulat

Electrochemical Proton Reduction over Nickel Foam for Z-Stereoselective Semihydrogenation/deuteration of Functionalized Alkynes

Valiente, Alejandro,Martínez-Pardo, Pablo,Kaur, Gurpreet,Johansson, Magnus J.,Martín-Matute, Belén

, (2021/12/22)

Selective reduction strategies based on abundant-metal catalysts are very important in the production of chemicals. In this paper, a method for the electrochemical semihydrogenation and semideuteration of alkynes to form Z-alkenes was developed, using a simple nickel foam as catalyst and H3O+ or D3O+ as sources of hydrogen or deuterium. Good yields and excellent stereoselectivities (Z/E up to 20 : 1) were obtained under very mild reaction conditions. The reaction proceeded with terminal and nonterminal alkynes, and also with alkynes containing easily reducible functional groups, such as carbonyl groups, as well as aryl chlorides, bromides, and even iodides. The nickel-foam electrocatalyst could be recycled up to 14 times without any change in its catalytic properties.

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