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α-Ethyl-4-chloro-α-methyldihydrocinnamic acid is a complex organic chemical compound with the molecular formula C13H17ClO2. It is a derivative of dihydrocinnamic acid, featuring an ethyl group at the α-position, a chlorine atom at the 4-position, and a methyl group at the α-position as well. α-ethyl-4-chloro-α-methyldihydrocinnamic acid is characterized by its unique structure, which includes a cyclohexane ring with a double bond, a phenyl ring, and the aforementioned substituents. It is synthesized through various chemical reactions and is used in the pharmaceutical and chemical industries for the production of various drugs and intermediates. Due to its specific functional groups and structural features, it exhibits unique chemical properties and reactivity, making it a valuable compound for research and development in the field of organic chemistry.

67930-93-2

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67930-93-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67930-93-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,9,3 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67930-93:
(7*6)+(6*7)+(5*9)+(4*3)+(3*0)+(2*9)+(1*3)=162
162 % 10 = 2
So 67930-93-2 is a valid CAS Registry Number.

67930-93-2Downstream Products

67930-93-2Relevant 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

, p. 18 - 21 (2017)

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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