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α-Phenyl-o-methyl-zimtsaeure, also known as 3-(o-Tolyl)-2-phenyl-acrylsaeure, is a chemical compound that features a complex structure with a phenyl group attached to an o-methyl-zimtsaeure (o-methyl cinnamic acid) backbone. α-Phenyl-o-methyl-zimtsaeure, 3-(o-Tolyl)-2-phenyl-acrylsaeure is characterized by the presence of a phenyl ring and an o-tolyl group, which is a methyl-substituted phenyl ring. The molecule consists of a cinnamic acid structure with a phenyl group attached to the alpha position, and an o-tolyl group at the 3-position. This arrangement of functional groups gives the compound unique chemical properties and potential applications in various fields, such as pharmaceuticals or materials science, where its specific reactivity and structural features may be exploited.

22161-35-9

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22161-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22161-35-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,6 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22161-35:
(7*2)+(6*2)+(5*1)+(4*6)+(3*1)+(2*3)+(1*5)=69
69 % 10 = 9
So 22161-35-9 is a valid CAS Registry Number.

22161-35-9Downstream Products

22161-35-9Relevant academic research and scientific papers

Access to α,β-unsaturated carboxylic acids through water-soluble palladium catalyzed hydroxycarbonylation of alkynes using water as the solvent

Gao, Mingjie,Jia, Xiaofei,Lv, Jinhe,Ren, Xinyi,Song, Jiaxin,Xie, Congxia,Zhang, Jinrong,Zhang, Kai,Zhao, Jinyu,Zhou, Ziqin,Zong, Lingbo

, p. 4708 - 4713 (2021)

A sulfoxantphos modified palladium-catalyzed synthesis of α,β-unsaturated carboxylic acids from alkynes with CO and H2O was described. The atom-economic hydroxycarbonylation of various symmetrical and unsymmetrical alkynes can be achieved with chemo-, stereo-, and regioselectivity, affording the corresponding carboxylic acids in good to excellent yields. Using water as the reaction solvent, the water-soluble palladium catalyst was easily separated from the product and could be reused for 5 cycles.

Synthesis of Vinyl Carboxylic Acids using Carbon Dioxide as a Carbon Source by Iron-Catalyzed Hydromagnesiation

Santhoshkumar, Rajagopal,Hong, Ya-Chun,Luo, Ching-Zong,Wu, Yun-Ching,Hung, Chen-Hsun,Hwang, Kuen-Yuan,Tu, An-Pang,Cheng, Chien-Hong

, p. 2210 - 2213 (2016/07/19)

An iron-catalyzed synthesis of α,β-unsaturated carboxylic acids from alkynes and carbon dioxide was developed. This reaction proceeds through hydromagnesiation of alkynes followed by carbon dioxide insertion under atmospheric pressure and ambient temperature in the presence of iron and a Grignard reagent as a catalyst and hydride source, respectively. Several symmetrical and unsymmetrical alkynes were transformed into the corresponding acids in good to excellent yields. The methodology provides an efficient route to the synthesis of vinyl carboxylic acids.

GUANIDINE DERIVATIVES AS TRPC MODULATORS

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Page/Page column 42-43, (2014/02/16)

The present invention is directed to guanidine derivatives as inhibitors of transient receptor potential canonical channels (TRPC channels), in particular TRPC3 and/or TRPC6 and/or TRPC7 activity, more particularly TRPC6 activity. Also provided herein are processes for preparing compounds described herein, intermediates used in their synthesis, pharmaceutical compositions thereof, and methods for treating or preventing diseases, conditions and/or disorders mediated by TRPC channels (Formula (I))

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