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Thiophene, 2-(4-bromophenyl)-5-ethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

375826-33-8

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375826-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 375826-33-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,5,8,2 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 375826-33:
(8*3)+(7*7)+(6*5)+(5*8)+(4*2)+(3*6)+(2*3)+(1*3)=178
178 % 10 = 8
So 375826-33-8 is a valid CAS Registry Number.

375826-33-8SDS

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-bromophenyl)-5-ethoxythiophene

1.2 Other means of identification

Product number -
Other names Thiophene,2-(4-bromophenyl)-5-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:375826-33-8 SDS

375826-33-8Downstream Products

375826-33-8Relevant academic research and scientific papers

Troublesome alkoxythiophenes. A highly efficient synthesis via cyclization of γ-keto esters

Sonpatki,Herbert,Sandvoss,Seed

, p. 7283 - 7286 (2007/10/03)

A variety of alkoxythiophenes have been synthesized that represent ideal subunits for the synthesis of a new class of thermotropic liquid crystals via palladium-catalyzed cross-coupling reactions and organometallic derivatization. The methodology used represents the first highly efficient synthesis of alkoxythiophenes unlike previous pathways that have presented serious synthetic difficulties when the alkoxy chain consisted of more than four carbon atoms. The scope of the new procedure (relative to liquid crystalline intermediates) is presented and is compared and contrasted with the current literature.

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