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PropanaMide, 2-Methyl-N-(1-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72924-95-9

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72924-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72924-95-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,9,2 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72924-95:
(7*7)+(6*2)+(5*9)+(4*2)+(3*4)+(2*9)+(1*5)=149
149 % 10 = 9
So 72924-95-9 is a valid CAS Registry Number.

72924-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-N-(1-phenylethyl)propanamide

1.2 Other means of identification

Product number -
Other names N-(1-phenylethyl)isobutyramide

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:72924-95-9 SDS

72924-95-9Relevant academic research and scientific papers

Tropylium-promoted Ritter reactions

Doan, Son H.,Hussein, Mohanad A.,Nguyen, Thanh Vinh

supporting information, p. 8901 - 8904 (2021/09/10)

The Ritter reaction used to be one of the most powerful synthetic tools to functionalize alcohols and nitriles, providing valuableN-alkyl amide products. However, this reaction has not been frequently used in modern organic synthesis due to its employment of strongly acidic and harsh reaction conditions, which often lead to complicated side reactions. Herein, we report the development of a new method using salts of the tropylium ion to promote the Ritter reaction. This method works well on a range of alcohol and nitrile substrates, giving the corresponding products in good to excellent yields. This reaction protocol is amenable to microwave and continuous flow reactors, offering an attractive opportunity for further applications in organic synthesis.

Copper-Catalyzed Reductive N-Alkylation of Amides with N-Tosylhydrazones Derived from Ketones

Xu, Peng,Qi, Fu-Ling,Han, Fu-She,Wang, Yan-Hua

, p. 2030 - 2034 (2016/07/28)

A CuI-catalyzed reductive coupling of ketone-derived N-tosylhydrazones with amides is presented. Under the optimized conditions, an array of N-tosylhydrazones derived from aryl–alkyl and diaryl ketones could couple effectively with a wide variety of (hete

HIGH OXIDATION STATE TRANSITION METAL CARBOXYLATES AS ACYLATING AGENTS

Recht, Joel,Cohen, Brett I.,Goldman, Alan S.,Kohn, Joachim

, p. 7281 - 7284 (2007/10/02)

The formation of amide bonds from the reaction of metal carboxylates with amines was observed for the first time; complexes for titanium(IV), zirconium(IV) and tantalum(V) were investigated.

A CONVENIENT METHOD FOR THE SYNTHESIS OF CARBOXAMIDES AND PEPTIDES BY THE USE OF TETRABUTYLAMMONIUM SALTS

Watanabe, Yutaka,Mukaiyama, Teruaki

, p. 285 - 288 (2007/10/02)

Various carboxamides and peptides are prepared in good yields by treatment of free acids and amines in H2O-dichloromethane or aqueous THF with bis(o-nitrophenyl) phenylphosphonate in the presence of tetrabutylammonium hydrogen sulfate or bromide.Carboxylic esters are also successfully converted to amides via carboxylate salts in one-pot.

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