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α-(m-Methoxy-phenyl)-zimtsaeure, also known as α-(3-methoxyphenyl)-cinnamic acid, is a chemical compound that belongs to the class of cinnamic acids. It features a phenyl ring with a methoxy group at the meta position (third carbon) and a cinnamoyl group attached to the alpha carbon. This organic compound is characterized by its molecular formula C10H10O3 and a molar mass of 178.19 g/mol. It is a white crystalline solid and is soluble in organic solvents. α-(m-Methoxy-phenyl)-zimtsaeure has potential applications in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and reactivity.

94501-15-2

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94501-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94501-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,0 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 94501-15:
(7*9)+(6*4)+(5*5)+(4*0)+(3*1)+(2*1)+(1*5)=122
122 % 10 = 2
So 94501-15-2 is a valid CAS Registry Number.

94501-15-2Downstream Products

94501-15-2Relevant academic research and scientific papers

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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