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4-(4-methylphenyl)-3-phenyl-3-butene-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16736-13-3

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16736-13-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16736-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,3 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16736-13:
(7*1)+(6*6)+(5*7)+(4*3)+(3*6)+(2*1)+(1*3)=113
113 % 10 = 3
So 16736-13-3 is a valid CAS Registry Number.

16736-13-3Relevant academic research and scientific papers

Enantioselective synthesis of β-substituted chiral allylic amines: Via Rh-catalyzed asymmetric hydrogenation

Wang, Qingli,Gao, Wenchao,Lv, Hui,Zhang, Xumu

, p. 11850 - 11853 (2016/10/07)

An asymmetric mono-hydrogenation of 2-acetamido-1,3-dienes catalyzed by a Rh-DuanPhos complex has been developed. This approach provides easy access to chiral allylic amines with excellent enantioselectivities and high regioselectivities. The products are valuable chiral building blocks for pharmaceuticals.

Preparation of 1-methyl-3-phenylisoquinoline derivatives from oximes using polyphosphoric esters

Niemczak, Micha?,Czerniak, Kamil,Kopczyński, Tomasz

, p. 1868 - 1873 (2015/03/18)

We show a beneficial new approach to the preparation of 1-methyl-3-phenylisoquinoline derivatives. This method involves heating polyphosphate ester and the appropriate oximes obtained from 3,4-diphenylbut-3-en-2-one derivatives. The isoquinolines were syn

Substituted isoxazoles for the treatment of inflammation

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Page 39, (2010/11/30)

A class of substituted isoxazolyl compounds is described for use in treating inflammation and inflammation-related disorders. Compounds of particular interest are defined by Formula (III) wherein R7 is selected from hydroxyl, lower alkyl, carboxyl, halo, lower carboxylalkyl, lower alkoxycarbonylalkyl, lower alkoxyalkyl, lower carboxyalkoxyalkyl, lower haloalkyl, lower haloalkylsulfonyloxy, lower hydroxyalkyl, lower aryl (hydroxylalkyl), lower carboxyaryloxyalkyl, lower alkoxycarbonylaryloxyalkyl, lower cycloalkyl, lower cycloalkylalkyl, and lower aralkyl; and wherein R8 is one or more radicals independently selected from hydrido, lower alkylsulfinyl, lower alkyl, cyano, carboxyl, lower alkoxycarbonyl, lower haloalkyl, hydroxyl, lower hydroxyalkyl, lower haloalkoxy, amino, lower alkylamino, lower arylamino, lower aminoalkyl, nitro, halo, lower alkoxy, aminosulfonyl, and lower alkylthio; or a pharmaceutically-acceptable salt thereof.

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