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2-Propenamide, 2-(acetylamino)-N-methyl-3-phenyl-, (2E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

263874-95-9

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263874-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 263874-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,3,8,7 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 263874-95:
(8*2)+(7*6)+(6*3)+(5*8)+(4*7)+(3*4)+(2*9)+(1*5)=179
179 % 10 = 9
So 263874-95-9 is a valid CAS Registry Number.

263874-95-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-acetamido-N-methyl-3-phenylprop-2-enamide

1.2 Other means of identification

Product number -
Other names 2-Propenamide,2-(acetylamino)-N-methyl-3-phenyl-,(2E)

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:263874-95-9 SDS

263874-95-9Downstream Products

263874-95-9Relevant academic research and scientific papers

Synthesis of peptides with α,β-dehydroamino acids. XIII photoisomerization of Ac-(Z)-ΔpHe-NHMe: Ac-(E)-ΔPhe-NHMe

Kubica, Zbigniew,Kozlecki, Tomasz,Rzeszotarska, Barbara

, p. 296 - 297 (2000)

Easily accessible Ac-(Z)-ΔPhe-NHMe was photoisomerized to so far unknown Ac-(E)-ΔPhe-NHMe. Some parameters of the process leading to a diastereomeric mixture of ratio 90(Z): 10(E) have been tested and the photoisomerization has been carried out on a preparative milligram scale. The isomers were separated via crystallization followed by preparative HPLC.

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