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ethyl (2Z)-3-(acetylamino)-2-(4-nitrophenyl)-3-phenylacrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1147869-39-3

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1147869-39-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1147869-39-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,8,6 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1147869-39:
(9*1)+(8*1)+(7*4)+(6*7)+(5*8)+(4*6)+(3*9)+(2*3)+(1*9)=193
193 % 10 = 3
So 1147869-39-3 is a valid CAS Registry Number.

1147869-39-3SDS

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 ethyl (2Z)-3-(acetylamino)-2-(4-nitrophenyl)-3-phenylacrylate

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:1147869-39-3 SDS

1147869-39-3Relevant academic research and scientific papers

BF3 · Et2O-induced decomposition of ethyl 2-diazo-3-hydroxy-3,3-diarylpropanoates in acetonitrile: A novel approach to 2,3-diaryl β-enamino ester derivatives

Gioiello, Antimo,Venturoni, Francesco,Natalini, Benedetto,Pellicciari, Roberto

supporting information; experimental part, p. 3520 - 3523 (2009/09/30)

The BF3·Et2O-induced decomposition of ethyl 2-diazo-3-hydroxy-3,3-diarylpropanoates, prepared by the addition of a series of benzophenones to ethyl diazo(lithio)acetate, is reported and studied. By using acetonitrile as a solvent, the corresponding N-acyl β-enamino ester derivatives are obtained in good yields and with a diverse regioselectivity as the result of 1,2-aryl migration in the vinyl cation intermediates. The factors that govern the migratory aptitude as well as the mechanistic aspects of the reaction are discussed.

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