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1-[2-chloro-1-(4-methylphenyl)ethenyl]-4-methyl-benzene is a complex organic chemical compound with the molecular formula C16H15Cl. It is characterized by a benzene ring (C6H5) with a methyl group (CH3) attached at the 4th position. A second benzene ring is attached to the first through an ethene (C2H4) bridge, with the second benzene ring also having a methyl group at the 4th position. The ethene bridge has a chlorine atom (Cl) attached at the 2nd position. 1-[2-chloro-1-(4-methylphenyl)ethenyl]-4-methyl-benzene is likely to be used in the synthesis of various pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and functional groups.

5293-66-3

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5293-66-3 Usage

Explanation

The compound's full name, which describes its structure and composition.

Explanation

An alternative name for the compound, which is often used in a more informal context.

Explanation

The compound is classified as an organic compound, which means it contains carbon and hydrogen atoms.

Explanation

The core structure of the compound is a benzene ring, which is a six-carbon ring with alternating single and double bonds.

Explanation

The benzene ring has two substituents attached to it a 4-methyl group (a methyl group attached to the fourth carbon) and a 2-chloroethenyl group (a chlorinated ethene group attached to the second carbon).

Explanation

The compound is utilized in the manufacturing process of different industrial products, although the specific applications are not mentioned in the material.

Explanation

The compound is also used in the pharmaceutical industry, although the specific drugs or medications it is involved in are not provided in the material.

Explanation

Due to its chemical nature, it is important to take necessary safety measures when using or handling 1-[2-chloro-1-(4-methylphenyl)ethenyl]-4-methyl-benzene to prevent potential hazards or accidents.

Explanation

The chemical formula represents the compound's composition, with 15 carbon atoms, 13 hydrogen atoms, and 1 chlorine atom.

Type of Compound

Organic compound

Structure

Contains a benzene ring

Substituents

4-methyl group and 2-chloroethenyl group

Industrial Applications

Used in the production of various industrial products

Pharmaceutical Applications

Found in some pharmaceuticals

Safety Precautions

Handle with caution and follow proper safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 5293-66-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5293-66:
(6*5)+(5*2)+(4*9)+(3*3)+(2*6)+(1*6)=103
103 % 10 = 3
So 5293-66-3 is a valid CAS Registry Number.

5293-66-3Relevant academic research and scientific papers

Halogenation of 1,1-diarylethylenes by N-halosuccinimides

Zhang, Ge,Bai, Rui-Xue,Li, Chu-Han,Feng, Chen-Guo,Lin, Guo-Qiang

, p. 1658 - 1662 (2018/12/11)

An efficient method for the preparation of 2,2-diarylvinyl halides from the corresponding 1,1-diarylethylenes has been developed. N-Halosuccinimides (N-bromosuccinimide or N-chlorosuccinimide) were used as the halogenation reagents. The practicability of this method is highlighted by its simple operation, broad substrate scope and capability for large-scale reaction.

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