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N-butyl-2,2-diphenylacetamide is a chemical compound with the molecular formula C18H21NO. It is a white crystalline solid that is soluble in organic solvents. N-butyl-2,2-diphenylacetamide is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and herbicides. Its structure features a butyl group attached to a 2,2-diphenylacetamide moiety, which contributes to its reactivity and utility in chemical reactions. The compound is also known for its potential applications in the development of new materials and as a research tool in organic chemistry.

4107-02-2

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4107-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4107-02-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,0 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4107-02:
(6*4)+(5*1)+(4*0)+(3*7)+(2*0)+(1*2)=52
52 % 10 = 2
So 4107-02-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H21NO/c1-2-3-14-19-18(20)17(15-10-6-4-7-11-15)16-12-8-5-9-13-16/h4-13,17H,2-3,14H2,1H3,(H,19,20)

4107-02-2Relevant academic research and scientific papers

Method for treating conditions related to the glutamate receptor using carboxylic acid amide derivatives

-

, (2008/06/13)

The present invention is concerned with the use of carbonylamino derivatives of the formula wherein R signifies lower alkyl, lower alkenyl, lower alkinyl, cycloalkyl, lower alkoxy or CF3; R1signifies hydrogen or lower alkyl; R2and R3signify, independently from each other, hydrogen, halogen or nitro; Y signifies CH or N; n is 0-6; m is 0-2; as well as with their pharmaceutically acceptable salts for the treatment of diseases, which relate to metabotropic glutamate receptor antagonists and/or agonists.

Rearrangements of trihalomethyl ketones

Braverman, Samuel,Cherkinsky, Marina,Kumar, E. V. K. Suresh,Gottlieb, Hugo E.

, p. 4521 - 4529 (2007/10/03)

Trihalomethyl ketones have been prepared and their reactivity under basic conditions was investigated in terms of competition between 1,2- vs. 1,3-elimination and nucleophilic substitution. Favorskii rearrangement was the preferred process, but in those c

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