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4-Pentenamide, N-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52565-61-4

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52565-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52565-61-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,6 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52565-61:
(7*5)+(6*2)+(5*5)+(4*6)+(3*5)+(2*6)+(1*1)=124
124 % 10 = 4
So 52565-61-4 is a valid CAS Registry Number.

52565-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methylpent-4-enamide

1.2 Other means of identification

Product number -
Other names 4-Pentenamide,N-methyl

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:52565-61-4 SDS

52565-61-4Upstream product

52565-61-4Relevant academic research and scientific papers

Visible-Light-Mediated Synthesis of Amidyl Radicals: Transition-Metal-Free Hydroamination and N-Arylation Reactions

Davies, Jacob,Svejstrup, Thomas D.,Fernandez Reina, Daniel,Sheikh, Nadeem S.,Leonori, Daniele

, p. 8092 - 8095 (2016/07/16)

The development of photoredox reactions of aryloxy-amides for the generation of amidyl radicals and their use in hydroamination-cyclization and N-arylation reactions is reported. Owing to the ease of single-electron-transfer reduction of the aryloxy-amides, the organic dye eosin Y was used as the photoredox catalyst, which results in fully transition-metal-free processes. These transformations exhibit a broad scope, are tolerant to several important functionalities, and have been used in the late-stage modification of complex and high-value N-containing molecules.

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