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Benzenepropanamide, N,N-dibutyl-, also known as N,N-Dibutylbenzenepropanamide, is an organic compound with the chemical formula C17H27NO. It is a derivative of benzenepropanamide, where two butyl groups are attached to the nitrogen atom. This colorless to pale yellow liquid is soluble in organic solvents and has a molecular weight of 259.4 g/mol. It is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its potential applications in the production of drugs and other products, it is an important compound in the field of organic chemistry.

57772-72-2

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57772-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57772-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,7,7 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57772-72:
(7*5)+(6*7)+(5*7)+(4*7)+(3*2)+(2*7)+(1*2)=162
162 % 10 = 2
So 57772-72-2 is a valid CAS Registry Number.

57772-72-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dibutyl-3-phenylpropanamide

1.2 Other means of identification

Product number -
Other names N,N-dibutyl-3-phenyl-propionamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57772-72-2 SDS

57772-72-2Relevant academic research and scientific papers

Catalyzation of 1,4-additions of arylboronic acids to α,β- unsaturated substrates using nickel(I) complexes

Meng, Jing-Jing,Gao, Min,Dong, Min,Wei, Yu-Ping,Zhang, Wen-Qin

, p. 2107 - 2109 (2014/04/03)

Nickel(I) complexes were generated in situ from Ni (PPh3) 2Cl2 using activated iron and the complexes combined with N,N′-bis(4-fluorobenzylidene) ethane-1,2-diamine (BFBED) were then used as a catalyst for the 1,4-addition reaction of arylboronic acids to α,β-unsaturated substrates. The reaction proceeded to completion and did not require the addition of a base but the addition of potassium iodide is crucial to this cross-coupling reaction. Moreover, experimental observations suggested a possible Ni(I)-Ni(III) catalytic cycle mechanism.

A SIMPLE METHOD FOR SYNTHESIS OF AMIDES AND PEPTIDES THROUGH ACYL CHLORIDES. A RAPID SYNTHESIS OF THYROTROPIN RELEASING HORMONE

Matsuda, Fuyuhiko,Itoh, Shin,Hattori, Noritaka,Yanagiya, Mitsutoshi,Matsumoto, Takeshi

, p. 3625 - 3631 (2007/10/02)

By improvement of the classical SOCl2-pyridine method for the preparation of acid chlorides, amides and optically pure peptides were synthesized rapidly in a simple manner from DCHA (dicyclohexylammonium) salts of carboxylic acids.This modified SOCl2-pyridine method was applied to a rapid synthesis of TRH.

SYNTHESIS AND PROPERTIES OF SOME N,N,-DIALKYLAMIDES AS NEW EXTRACTANTS.

Al-Jallo,Hussain,Mansoor,Sameh,Al-Saidi

, p. 479 - 481 (2007/10/02)

Forty-seven new N,N-dialkylamides were prepared and their physical and spectral data are tabulated. The solubility of amides 1-47 in organic and aqueous solvents was tested and the results showed that as the amides are freely soluble in organic solvents t

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