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2-ethoxythiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

36448-24-5

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36448-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 36448-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,4,4 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36448-24:
(7*3)+(6*6)+(5*4)+(4*4)+(3*8)+(2*2)+(1*4)=125
125 % 10 = 5
So 36448-24-5 is a valid CAS Registry Number.

36448-24-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethoxythiophene

1.2 Other means of identification

Product number -
Other names Thiophene,2-ethoxy

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:36448-24-5 SDS

36448-24-5Relevant articles and documents

METHOD OF SYNTHESIS OF 5,6?BIS(5?ALKOXYTHIOPHEN?2?YL)PYRAZINE-2,3-DICARBONITRILES, DERIVATIVES OF DICYANOPYRAZINE AND USE THEREOF

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Page/Page column 7; 8, (2019/10/19)

The present invention relates to a method of synthesis of compounds of general formula (I) wherein R is linear or branched (C1-C8) alkyl, (C5-C6) cycloalkyl or benzyl, the method comprising the following steps: 10 step a) Friedel-Crafts reaction of thioph

Practical Ligand-Free Copper-Catalysed Short-Chain Alkoxylation of Unactivated Aryl Bromides

Guo, Ying,Fan, Xue-Min,Nie, Min,Liu, Hong-Wei,Liao, Dao-Hua,Pan, Xian-Dao,Ji, Ya-Fei

, p. 4744 - 4755 (2015/08/03)

An efficient and practical short-chain alkoxylation of unactivated aryl bromides has been developed with special attention focussed on the applicability of the reaction. Sodium alkoxide is used as the nucleophile, and the corresponding alcohol as the solvent. The reaction requires neither precious metals nor organic ligands. It uses a catalytic system consisting of copper(I) bromide as a catalyst, the corresponding alkyl formate as a noncontaminating cocatalyst, and lithium chloride as an additive. A wide range of substrates and test cases highlight the synthetic utility of the approach. Considering the commercial accessibility and affordability of the feedstocks, this protocol shows promise as a new alternative for the sustainable preparation of aryl alkyl ethers.

ANTIBACTERIAL AGENTS: ARYL MYXOPYRONIN DERIVATIVES

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Page/Page column 89, (2014/01/09)

The invention provides compounds of formula la, lb and Ic: [Formula Ia, Ib, and Ic] and salts thereof, wherein variables are as described in the specification, as well as compositions comprising a compound of formula Ia-Ic, methods of making such compounds, and methods of using such compounds, e.g., as inhibitors of bacterial RNA polymerase and as antibacterial agents.

PHOTOCHROMIC MATERIAL

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Page 9, (2008/06/13)

A photochromic material having a ring opening quantum yield of 10-3 or lower which does not fade under ambient light is provided. The material comprises a compound belonging to the diheteroarylethene class. The compound has alkoxy group and ary

Antitumor compositions and methods of treatment

-

, (2008/06/13)

This invention provides certain sulfonamide compounds, formulations and method of use of certain sulfonamide compounds in treating susceptible neoplasms.

Copper(I) Halide Catalysed Synthesis of Alkyl Aryl and Alkyl Heteroaryl Ethers

Keegstra, Menno A.,Peters, Theo H. A.,Brandsma, Lambert

, p. 3633 - 3652 (2007/10/02)

A number of alkyl aryl and alkyl heteroaryl ethers have been prepared from (hetero) aryl halides (mainly bromides) and sodium alkoxides, using copper(I)bromide as a catalyst.The influence of the main solvent, the halogen atom, reaction temperature and the presence of oxygen upon the rate and selectivity has been studied.Furthermore the decomposition of the catalyst and the reduction of the aryl halide are studied.

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