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α-Methylzimtsaeureanilid, also known as α-methyl cinnamic acid anilide, is an organic compound with the chemical formula C15H15NO. It is a derivative of cinnamic acid, featuring a methyl group attached to the cinnamic acid structure and an aniline group (phenylamine) connected to it. α-Methylzimtsaeureanilid is characterized by its aromatic properties and is often used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its versatile chemical structure. It plays a significant role in the chemical industry as an intermediate in the production of various compounds, showcasing its importance in the field of organic chemistry.

71099-84-8

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71099-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71099-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,9 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 71099-84:
(7*7)+(6*1)+(5*0)+(4*9)+(3*9)+(2*8)+(1*4)=138
138 % 10 = 8
So 71099-84-8 is a valid CAS Registry Number.

71099-84-8Relevant academic research and scientific papers

Metal-free synthesis of 3,3-disubstituted oxoindoles by iodine(III)-catalyzed bromocarbocyclizations

Fabry, David C.,Stodulski, MacIej,Hoerner, Stefanie,Gulder, Tanja

, p. 10834 - 10838 (2012)

"I" did it: An iodine(III)-mediated bromocarbocyclization was elaborated as an efficient tool for the synthesis of oxoindoles. This method is applicable to a variety of structurally different substrates, also with chemically sensitive groups, and gives access to the heterocycles in a regio- and stereoselective fashion (see scheme). The indole-2-ones obtained can be converted easily into structurally complex target compounds, such as the alkaloid physostigmine. Copyright

Highly enantioselective construction of the α-chiral center of amides via iridium-catalyzed hydrogenation of α,β-unsaturated amides

Lu, Wei-Jing,Hou, Xue-Long

supporting information; experimental part, p. 1224 - 1228 (2009/12/06)

The chiral center at the a-position of amides is installed in excellent enantioselectivity via the iridium-catalyzed asymmetric hydrogenation of αβ-unsaturated amides under mild conditions. Even aliphatic amides are suitable substrates. The presence of a

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