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1-Cyclopentene-1-carboxylic acid, 2-[(4-methoxyphenyl)amino]-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94091-87-9

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94091-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94091-87-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,9 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94091-87:
(7*9)+(6*4)+(5*0)+(4*9)+(3*1)+(2*8)+(1*7)=149
149 % 10 = 9
So 94091-87-9 is a valid CAS Registry Number.

94091-87-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenylamino)-cyclopent-1-enecarboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names ethyl 2-(4-methoxyphenylamino)cyclopent-1-enecarboxylate

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:94091-87-9 SDS

94091-87-9Relevant academic research and scientific papers

General, mild and efficient synthesis of β-enaminones catalyzed by ceric ammonium nitrate

Sridharan, Vellaisamy,Avenda?o, Carmen,Menéndez

, p. 881 - 884 (2008/02/02)

Ceric ammonium nitrate catalyzes the reaction between aromatic or aliphatic primary amines and a variety of β-dicarbonyl compounds, including β-ketoesters, β-ketothioesters and β-diketones. The reaction proceeds smoothly at room temperature in short react

ZrCl4-catalyzed efficient synthesis of enaminones and enamino esters under solvent-free conditions

Lin, Jin,Zhang, Li-Feng

, p. 77 - 81 (2007/10/03)

A facile synthesis of β-enaminones and enamino esters by condensation of β-dicarbonyl compounds with differently substituted amines in the presence of ZrCl4 under solvent-free conditions is reported.

Phosphotungstic acid catalysed synthesis of β-enamino compounds under solvent-free conditions

Li, Geng-Chen

, p. 696 - 698 (2008/09/20)

A convenient eco-friendly procedure has been developed for the synthesis of β-enaminones and β-enamino esters by reacting 1,3-dicarbonyl compounds with amines in the presence of catalytic amounts of phosphotungstic acid (H3PW12O40,1 mol%). The reaction proceeds smoothly at room temperature under solvent-free conditions and gives the corresponding β-enamino compounds in high to excellent yields.

A general and efficient method for the preparation of β-enamino ketones and esters catalyzed by indium tribromide

Zhang, Zhan-Hui,Yin, Liang,Wang, Yong-Mei

, p. 184 - 190 (2007/10/03)

A variety of β-enamino ketones and esters have been synthesized in high to exellent yields by reacting β-dicarbonyl compounds with amines in the presence of a catalytic amount of indium tribromide. The reaction proceeds smoothly at room temperature in a short reaction time under solvent-free conditions.

A solvent-free synthesis of β-amino-α,β-unsaturated ketones and esters catalysed by sulfated zirconia

Zhang, Zhan-Hui,Song, Li-Ming

, p. 817 - 820 (2007/10/03)

β-Amino-α,β-unsaturated ketones and esters are synthesised by the condensation of β-dicarbonyl compounds with amines in the presence of a solid superacid sulfated zirconia (SO42-/ZrO 2, SZ) under solvent-free conditions.

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