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2-Propenoic acid, 2-(acetylamino)-3-(4-cyanophenyl)-, methyl ester, (2Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

556829-03-9

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556829-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 556829-03-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,8,2 and 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 556829-03:
(8*5)+(7*5)+(6*6)+(5*8)+(4*2)+(3*9)+(2*0)+(1*3)=189
189 % 10 = 9
So 556829-03-9 is a valid CAS Registry Number.

556829-03-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 2-acetamido-3-(4-cyanophenyl)prop-2-enoate

1.2 Other means of identification

Product number -
Other names -

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:556829-03-9 SDS

556829-03-9Downstream Products

556829-03-9Relevant academic research and scientific papers

Silver-Promoted Direct Phosphorylation of Bulky C(sp2)-H Bond to Build Fully Substituted β-Phosphonodehydroamino Acids

Cao, Hao-Qiang,Liu, Hao-Nan,Liu, Zhe-Yuan,Qiao, Baokun,Zhang, Fa-Guang,Ma, Jun-An

, p. 6414 - 6419 (2020/09/02)

A general and practical cross-dehydrogenative coupling protocol between readily available trisubstituted α,β-dehydro α-amino carboxylic esters and H-phosphites is described. This C(sp2)-H phosphorylation reaction proceeds with absolute Z-selectivity promoted by silver salt in a radical relay manner. The bulky tetrasubstituted β-phosphonodehydroamino acids were obtained in grams and added new modules to the toolkit for peptide modifications.

Ligand-free palladium catalysed Heck reaction of methyl 2-acetamido acrylate and aryl bromides as key step in the synthesis of enantiopure substituted phenylalanines

Willans, Charlotte E.,Mulders, Jan M.C.A.,de Vries, Johannes G.,de Vries, André H.M.

, p. 494 - 497 (2007/10/03)

A range of substituted aryl bromides were coupled with methyl 2-acetamido acrylate using ligand-free palladium catalysis. Subsequently asymmetric hydrogenation with Rh/MonoPhos yielded substituted phenylalanines in high enantioselectivities (e.e. 92-99%).

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