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2-(2-chlorophenyl)-3-phenylpropionic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108476-39-7

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108476-39-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108476-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,4,7 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 108476-39:
(8*1)+(7*0)+(6*8)+(5*4)+(4*7)+(3*6)+(2*3)+(1*9)=137
137 % 10 = 7
So 108476-39-7 is a valid CAS Registry Number.

108476-39-7Downstream Products

108476-39-7Relevant academic research and scientific papers

Visible-Light-Driven Reductive Carboarylation of Styrenes with CO2 and Aryl Halides

Gao, Yuzhen,Li, Gang,Wang, Hao,Zhou, Chunlin

supporting information, p. 8122 - 8129 (2020/05/20)

The first example of visible-light-driven reductive carboarylation of styrenes with CO2 and aryl halides in a regioselective manner has been achieved. A broad range of aryl iodides and bromides were compatible with this reaction. Moreover, pyridyl halides, alkyl halides, and even aryl chlorides were also viable with this method. These findings may stimulate the exploration of novel visible-light-driven Meerwein arylation-addition reactions with user-friendly aryl halides as the radical sources and the photocatalytic utilization of CO2

Reactions of chlorine substituted (E)-2,3-diphenylpropenoic acids over cinchonidine-modified Pd: Enantioselective hydrogenation versus hydrodechlorination

Szllsi, Gy?rgy,Hermán, Beáta,Szabados, Erika,Fül?p, Ferenc,Bartók, Mihály

experimental part, p. 28 - 36 (2011/02/24)

The effect of the chlorine position on the C-Cl bond hydrogenolysis and the enantioselective hydrogenation of Cl substituted (E)-2,3-diphenylpropenoic acid derivatives has been studied over cinchonidine-modified Pd/Al2O 3. In contrast to the fast hydrodechlorination of the β-phenyl-para-Cl substituted acids the Cl on the α-phenyl ring was barely hydrogenolized. These observations were interpreted by the different arrangements of the two phenyl rings on the surface, with the α- and β-phenyl rings adsorbed tilted and parallel, respectively. The results confirmed the beneficial effect of the α-phenyl-ortho-substituents on the chiral discrimination, thus the 2,3-diphenylpropionic acids substituted by Cl on the α-phenyl ring could be prepared in good yields and optical purities. The conclusions were used for the rational design of an acid, i.e. (E)-2-(2-methoxyphenyl)-3-(3,4-difluorophenyl)propenoic acid, which afforded the best optical purity (ee up to 95% at 295 K) described until now in this heterogeneous system.

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