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203730-54-5

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203730-54-5 Usage

General Description

2-Ethylaminothiophene is a chemical compound with the molecular formula C6H9NS. It is a thiophene derivative with an ethylamino functional group attached to the 2-position of the thiophene ring. 2-Ethylaminothiophene is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and organic materials. 2-Ethylaminothiophene has shown potential applications in the development of organic electronic devices such as organic light-emitting diodes and organic photovoltaics due to its electronic and optoelectronic properties. It is also used as a key intermediate in the production of dyes, pigments, and polymers. Additionally, this compound is known for its unique aromatic and sulfur-containing properties, which make it valuable in the synthesis of diverse chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 203730-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,7,3 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 203730-54:
(8*2)+(7*0)+(6*3)+(5*7)+(4*3)+(3*0)+(2*5)+(1*4)=95
95 % 10 = 5
So 203730-54-5 is a valid CAS Registry Number.

203730-54-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethylthiophen-2-amine

1.2 Other means of identification

Product number -
Other names thien-2-ylethylamine

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:203730-54-5 SDS

203730-54-5Relevant articles and documents

One-pot syntheses of 2-N-Alkylamino-, 2-N-Phenylamino-2-N,N-Dialkylamino-, and 2-N-Alkyl-N-phenylaminothiophenes

Tarasova, Olga A.,Klyba, Ludmila V.,Vvedensky, Vladimir Yu.,Nedolya, Nina A.,Trofimov, Boris A.,Brandsma, Lambert,Verkruijsse, Hermann D.

, p. 253 - 256 (1998)

A number of 2-N-alkylamino- or 2-N-phenylamino-, 2-N,N-dialkylamino-, and 2-N-alkyl-N-phenylaminothiophenes have been prepared in good yields by adding a solution of tert-butylalcohol and potassium tert-butoxide in dimethylsulfoxide to a solution of the adduct from a lithiated 1-alkyne, RCH2C≡CLi, or the lithiated allene, tBuCH=C=CHLi, and isothiocyanate, R′N=C=S, in tetrahydrofuran and subsequently hydrolyzing the reaction mixture or quenching it with methyl iodide.

Oligomeric aminodiol-containing compounds, libraries thereof, and process of preparing the same

-

, (2008/06/13)

Oligomeric compounds comprising a plurality of aminodiol monomer subunits joined by linking groups are provided, as well as libraries of such compounds and processes for preparing the oligomeric compounds and libraries.

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