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N-(1-Isoquinolinyl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33357-47-0

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33357-47-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33357-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,5 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33357-47:
(7*3)+(6*3)+(5*3)+(4*5)+(3*7)+(2*4)+(1*7)=110
110 % 10 = 0
So 33357-47-0 is a valid CAS Registry Number.

33357-47-0SDS

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-isoquinolin-1-ylbenzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-1-isoquinolyl

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:33357-47-0 SDS

33357-47-0Relevant academic research and scientific papers

Mild and direct conversion of quinoline N-oxides to 2-amidoquinolines with primary amides

Couturier, Michel,Caron, Laurence,Tumidajski, Stephanie,Jones, Kris,White, Timothy D.

, p. 1929 - 1932 (2007/10/03)

A simple, one-pot procedure is described for the direct conversion of quinoline N-oxides to α-amidoquinolines with primary amides. This methodology is complimentary to the Abramovich reaction, which is limited to the introduction of secondary amides via imidoyl chlorides. Although reaction conditions are quite similar, omission of the base is key for successful reaction with primary amides, which were found not to proceed through the intermediacy of an imidoyl chloride but rather through an acyl isocyanate.

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