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β,β-Dichloro-3'-methyl-styrene is an organic chemical compound with the molecular formula C9H8Cl2. It is a colorless to pale yellow liquid with a pungent odor. β,β-dichloro-3'-methyl-styrene is characterized by the presence of a styrene backbone, which includes a vinyl group (C=C) and a phenyl ring, with a methyl group attached to the 3' position of the phenyl ring. Additionally, it has two chlorine atoms attached to the β-carbon of the vinyl group, which are in the same relative position. This chemical is primarily 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 β,β-dichloro-3'-methyl-styrene with care, following proper safety protocols to minimize potential health and environmental risks.

65085-90-7

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65085-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65085-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,8 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65085-90:
(7*6)+(6*5)+(5*0)+(4*8)+(3*5)+(2*9)+(1*0)=137
137 % 10 = 7
So 65085-90-7 is a valid CAS Registry Number.

65085-90-7Downstream Products

65085-90-7Relevant academic research and scientific papers

A Robust One-Step Approach to Ynamides

Tu, Yongliang,Zeng, Xianzhu,Wang, Hui,Zhao, Junfeng

supporting information, p. 280 - 283 (2018/01/17)

A robust one-step synthetic strategy for ynamide with cheap and easily available stock chemicals vinyl dichlorides and electron deficient amides as the starting material is described. In the absence of transition-metal catalyst, the reaction proceeds under mild reaction conditions in open air and thus rendering a convenient operation. This strategy is not only suitable for both terminal and internal ynamide synthesis but also amenable for large-scale preparation. Broad substrate scopes with respect to vinyl dichloride as well as electron-deficient amide were observed.

Reduction of trihalomethyl carbinols and their acetates, mesylates and tosylates by indium metal

Ranu, Brindaban C.,Samanta, Sampak,Das, Arijit

, p. 5993 - 5995 (2007/10/03)

A study of reduction of trihalomethyl carbinols and their derivatives by indium metal shows that while trichloromethyl carbinols produce a mixture of the corresponding dichloromethyl carbinol and vinylidene dichloride, the acetates, mesylates and tosylate

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