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Ethanol, 2-[(4-ethoxyphenyl)amino]-, also known as 2-(4-ethoxyphenylamino)ethanol or 4-ethoxyphenethylamine, is an organic compound with the chemical formula C10H15NO2. It is a colorless liquid with a molecular weight of 181.23 g/mol. Ethanol, 2-[(4-ethoxyphenyl)amino]- is an ethanol derivative featuring an amino group attached to the 2-position and a 4-ethoxyphenyl group at the same position. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential applications, it is essential to handle this chemical with care, following proper safety guidelines and regulations.

2933-80-4

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2933-80-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2933-80-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,3 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2933-80:
(6*2)+(5*9)+(4*3)+(3*3)+(2*8)+(1*0)=94
94 % 10 = 4
So 2933-80-4 is a valid CAS Registry Number.

2933-80-4SDS

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 2-(4-ethoxyphenylamino)ethanol

1.2 Other means of identification

Product number -
Other names 4-(β-Oxy-aethylamino)-phenetol

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:2933-80-4 SDS

2933-80-4Relevant academic research and scientific papers

BmimOAc ionic liquid: A highly efficient catalyst for synthesis of 3-aryl-2-oxazolidinones by direct condensation of 2-(arylamino) alcohols with diethyl carbonate

Elageed, Elnazeer H.M.,Wang, Binshen,Zhang, Yongya,Wu, Shi,Gao, Guohua

, p. 271 - 277 (2015/09/01)

An efficient convenient procedure for the synthesis of 3-aryl-2-oxazolidinones from 2-(arylamino) alcohols and diethyl carbonate (DEC) catalyzed by ionic liquids is described. The effects of reaction time, amount of catalyst and temperature were investigated. Excellent yields of products were obtained under the optimized reaction conditions, when using BmimOAc as a catalyst. An intermediate ethyl 2-(phenyl amino) ethyl carbonate was isolated and characterized. 1H NMR spectroscopy and DFT calculations indicated that BmimOAc cooperatively activate the substrates through hydrogen bonding with its anion and cation sites. According to these results, a possible reaction mechanism was discussed.

Lewis acids catalyzed ring-opening reactions of methylenecyclopropanes and epoxides in supercritical carbon dioxide or modified supercritical carbon dioxide with perfluorocarbon

Shi, Min,Chen, Yu

, p. 219 - 227 (2007/10/03)

The reactions of methylenecyclopropanes (MCPs) and epoxides with alcohols and aromatic amines can be carried out in supercritical carbon dioxide (scCO2) or modified scCO2 with perfluorocarbon which offer a way to synthesize various alcohols, amino-alcohols, homoallylic ethers, and amines under an environmentally benign condition.

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