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Benzamide, N-(cyclopropylcarbonyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

756488-67-2

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756488-67-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 756488-67-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,5,6,4,8 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 756488-67:
(8*7)+(7*5)+(6*6)+(5*4)+(4*8)+(3*8)+(2*6)+(1*7)=222
222 % 10 = 2
So 756488-67-2 is a valid CAS Registry Number.

756488-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(cyclopropanecarbonyl)benzamide

1.2 Other means of identification

Product number -
Other names cyclopropanecarboxylic acid benzoylamide

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:756488-67-2 SDS

756488-67-2Downstream Products

756488-67-2Relevant academic research and scientific papers

Vanadium-Catalyzed Oxidative C(CO)-C(CO) Bond Cleavage for C-N Bond Formation: One-Pot Domino Transformation of 1,2-Diketones and Amidines into Imides and Amides

Digwal, Chander Singh,Yadav, Upasana,Ramya, P. V. Sri,Sana, Sravani,Swain, Baijayantimala,Kamal, Ahmed

, p. 7332 - 7345 (2017/07/26)

A novel vanadium-catalyzed one-pot domino reaction of 1,2-diketones with amidines has been identified that enables their transformation into imides and amides. The reaction proceeds by dual acylation of amidines via oxidative C(CO)-C(CO) bond cleavage of 1,2-diketones to afford N,N′-diaroyl-N-arylbenzamidine intermediates. In the reaction, these intermediates are easily hydrolyzed into imides and amides through vanadium catalysis. This method provides a practical, simple, and mild synthetic approach to access a variety of imides as well as amides in high yields. Moreover, one-step construction of imide and amide bonds with a long-chain alkyl group is an attractive feature of this protocol.

Novel chromium(VI) catalyzed oxidation of N-alkylamides to imides with periodic acid

Xu, Liang,Zhang, Suhong,Trudell, Mark L.

, p. 1668 - 1669 (2007/10/03)

A novel and practical procedure for preparation of imides is described using chromium(VI) oxide to catalyze the oxidation of N-alkylamides with periodic acid in the presence of acetic anhydride in acetonitrile.

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