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N-benzyl-3-(benzylamino)-3-phenylpropanamide is a complex organic compound with the molecular formula C26H26N2O. It is a derivative of propanamide, featuring a benzyl group attached to the nitrogen atom, and a benzylamino group connected to the third carbon. The molecule also contains a phenyl group attached to the same carbon as the benzylamino group. N-benzyl-3-(benzylamino)-3-phenylpropanamide is known for its potential applications in pharmaceutical research, particularly in the development of drugs targeting the dopamine D2 receptor. Its structure allows for interactions with biological targets, making it a subject of interest in medicinal chemistry. The specific properties and uses of N-benzyl-3-(benzylamino)-3-phenylpropanamide are under ongoing investigation, with the aim of understanding its therapeutic potential and optimizing its structure for various medical applications.

5100-01-6

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5100-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5100-01-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,0 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5100-01:
(6*5)+(5*1)+(4*0)+(3*0)+(2*0)+(1*1)=36
36 % 10 = 6
So 5100-01-6 is a valid CAS Registry Number.

5100-01-6Downstream Products

5100-01-6Relevant academic research and scientific papers

[2+2] Cycloaddition reactions of 1-benzyl-2,4-diphenyl-1,3-diazabuta-1,3-diene with chiral ketenes

Abbiati, Giorgio,Rossi, Elisabetta

, p. 7205 - 7212 (2001)

The [2+2] cycloaddition reactions of 1-benzyl-2,4-diphenyl-1,3-diaza-1,3-butadiene with β-(dimethylphenylsilyl)ketene, β-menthoxyketene and Evans-Sjo?gren ketene were investigated. The results and some chemical transformations of the obtained cycloadducts

A solid-supported arylboronic acid catalyst for direct amidation

Du, Yihao,Barber, Thomas,Lim, Sol Ee,Rzepa, Henry S.,Baxendale, Ian R.,Whiting, Andrew

supporting information, p. 2916 - 2919 (2019/03/27)

An efficient heterogeneous amidation catalyst has been prepared by co-polymerisation of styrene, DVB with 4-styreneboronic acid, which shows wide substrate applicability and higher reactivity than the equivalent homogeneous phenylboronic acid, suggesting potential cooperative catalytic effects. The catalyst can be easily recovered and reused; suitable for use in packed bed flow reactors.

Practical, highly enantioselective chemoenzymatic one-pot synthesis of short-chain aliphatic β-amino acid esters

Wei?, Markus,Gr?ger, Harald

experimental part, p. 1251 - 1254 (2009/09/06)

A practical, highly enantioselective method for the synthesis of short-chain aliphatic β-amino acid esters was developed starting from prochiral and easily accessible substrates. This chemoenzymatic approach is based on a nonenzymatic aza-Michael addition

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