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α-Ethyl-α-methyl-4-chloro-dihydrocinnamic acid methyl ester is a complex organic compound with the chemical formula C13H17ClO2. It is a derivative of dihydrocinnamic acid, featuring an ethyl group at the α-position, a methyl group at the α-position, and a chlorine atom at the 4-position. The molecule is further characterized by the presence of a methyl ester group, which is attached to the carboxylic acid functionality. α-ethyl-α-methyl-4-chloro-dihydrocinnamic acid methyl ester is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of various biologically active molecules. Its structure provides a foundation for further chemical modifications, making it a valuable component in the development of new drugs and chemical compounds.

57145-18-3

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57145-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57145-18-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,1,4 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 57145-18:
(7*5)+(6*7)+(5*1)+(4*4)+(3*5)+(2*1)+(1*8)=123
123 % 10 = 3
So 57145-18-3 is a valid CAS Registry Number.

57145-18-3Relevant academic research and scientific papers

Nickel-Catalyzed oxidative coupling of unactivated C(sp3)-H bonds in aliphatic amides with terminal alkynes

Luo, Fei-Xian,Cao, Zhi-Chao,Zhao, Hong-Wei,Wang, Ding,Zhang, Yun-Fei,Xu, Xing,Shi, Zhang-Jie

supporting information, p. 18 - 21 (2017/04/04)

In this work, we demonstrated Ni-catalyzed oxidative coupling of unactivated C(sp3)-H bonds with terminal alkynes for construction of C(sp3)-C(sp) bonds to synthesize alkyl-substituted internal alkynes. Different amides exhibited good compatibility. Preliminary mechanistic studies were conducted to account for this alkynylation.

Indaneacetic acid derivatives

-

, (2008/06/13)

This invention provides new compounds of formula I, STR1 wherein R1 is lower alkyl, R2 is hydrogen or lower alkyl, R3 is hydrogen or lower alkyl, R4 is hydrogen or lower alkyl, R5 is hydrogen, chlorine or lower alkyl, and each of R6 and R7 is hydrogen, or, when R5 is hydrogen, R6 may also be chlorine or lower alkyl, and R7 chlorine or lower alkyl, Useful as anti-phlogistic and anti-arthritic agents.

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