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2-methylene-5-phenylvaleric acid chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78574-19-3

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78574-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78574-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,7 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78574-19:
(7*7)+(6*8)+(5*5)+(4*7)+(3*4)+(2*1)+(1*9)=173
173 % 10 = 3
So 78574-19-3 is a valid CAS Registry Number.

78574-19-3Relevant academic research and scientific papers

Ni-Catalyzed enantioselective reductive arylcyanation/cyclization of: N -(2-iodo-aryl) acrylamide

Dong, Kaiwu,Ren, Xinyi,Shen, Chaoren,Wang, Guangzhu

, p. 1135 - 1138 (2022/02/03)

A Ni/(S,S)-BDPP-catalyzed intramolecular Heck cyclization of N-(2-iodo-aryl) acrylamide with 2-methyl-2-phenylmalononitrile was developed to give oxindoles with good enantioselectivities. We found that utilizing such an electrophilic cyanation reagent cou

Stereoselective synthesis of Z-vinylsilanes via palladium-catalyzed direct intermolecular silylation of C(sp2)-H bonds

Pan, Jin-Long,Chen, Chao,Ma, Zhi-Gang,Zhou, Jia,Wang, Li-Ren,Zhang, Shu-Yu

supporting information, p. 5216 - 5219 (2017/11/06)

An efficient and convenient palladium-catalyzed direct intermolecular silylation of C(sp2)-H bonds by using disilanes as the silicon source with the assistance of a readily removable bidentate directing group is reported. This strategy provided a regio- and stereoselective protocol for exclusive synthesis of Z-vinylsilanes with reasonable to excellent yields and good functional group compatibility. Silylation of the isolated palladacycle intermediate revealed the Z-stereoselective pathway. Moreover, the practicality and effectiveness of this method were illustrated by a gram-scale experiment and further functionalization of the silylation product.

Synthesis and Hypoglycemic Activity of Phenylalkyloxiranecarboxylic Acid Derivatives

Eistetter, Klaus,Wolf, Horst P. O.

, p. 109 - 113 (2007/10/02)

A series of new 2-(phenylalkyl)oxirane-2-carboxylic acids has been synthesized and studied for its effects on the concentration of blood glucose.Most of the compounds exhibit remarkable blood glucose lowering activities in fasted rats.Structure-activity s

Substituted oxiranecarboxylic acids, their use and medicaments containing them

-

, (2008/06/13)

Substituted oxiranecarboxylic acids of the formula STR1 wherein R1 denotes a hydrogen atom (--H), a halogen atom, a hydroxylroup, a lower alkyl group, a lower alkoxy group or a trifluoromethyl group, R2 has one of the meanings of Rs

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