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N-benzyl-2-(3-benzylureido)benzamide is a complex organic compound with the molecular formula C22H21N3O2. It is a derivative of benzamide, featuring a benzyl group attached to the nitrogen atom and a 3-benzylureido group at the 2-position of the benzene ring. N-benzyl-2-(3-benzylureido)benzamide is characterized by its white crystalline appearance and is soluble in organic solvents. It is synthesized through a series of chemical reactions, typically involving the condensation of benzamide with appropriate benzylating agents. N-benzyl-2-(3-benzylureido)benzamide has potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various bioactive molecules and as a research tool in medicinal chemistry. Its structure and properties make it a valuable compound for exploring the structure-activity relationships of benzamide-based drugs.

2164-88-7

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2164-88-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2164-88-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2164-88:
(6*2)+(5*1)+(4*6)+(3*4)+(2*8)+(1*8)=77
77 % 10 = 7
So 2164-88-7 is a valid CAS Registry Number.

2164-88-7Downstream Products

2164-88-7Relevant academic research and scientific papers

Studies on the Lossen-type rearrangement of N-(3-phenylpropionyloxy) phthalimide and N-tosyloxy derivatives with several nucleophiles

Chanmiya Sheikh,Takagi, Shunsuke,Ogasawara, Asako,Ohira, Masayuki,Miyatake, Ryuta,Abe, Hitoshi,Yoshimura, Toshiaki,Morita, Hiroyuki

experimental part, p. 2132 - 2140 (2010/04/26)

The reaction of N-(3-phenylpropionyloxy)phthalimide (1a) and N-tosyloxy (5a,b) derivatives with nucleophiles was examined and found to give the products via Lossen-type rearrangement. In order to obtain the scope of this reaction mechanism, further studies the reaction of several N-sulfonyloxyimide derivatives with various nucleophiles under similar conditions were carried out and found to afford the corresponding same types of products in high yields.

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