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3-(4-METHOXYBENZOYL)-2-METHYLBENZOFURAN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94541-06-7

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94541-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94541-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,5,4 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 94541-06:
(7*9)+(6*4)+(5*5)+(4*4)+(3*1)+(2*0)+(1*6)=137
137 % 10 = 7
So 94541-06-7 is a valid CAS Registry Number.

94541-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methoxyphenyl)-(2-methyl-1-benzofuran-3-yl)methanone

1.2 Other means of identification

Product number -
Other names 2-Methyl-3-<p-methoxy-benzoyl>-benzofuran

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:94541-06-7 SDS

94541-06-7Relevant academic research and scientific papers

Preparation method of 2- (I)-3-methyl-benzoyl benzofuran (benzofuran) derivative

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Paragraph 0052-0055, (2019/11/18)

The invention discloses a preparation method of a 2-methyl-3-benzoylbenzofuran derivative. According to the preparation method, a 1-(phenylethynyl)-2-(ethylnenoxy)benzene substituendum is taken as rawmaterial, FeCl2 is taken as a catalyst, Phen is taken a

Synthesis of 2,3-disubstituted benzofurans on solid-support

Jung, Chun-Won,Shen, Liu-Lan,Choi, Brian Hyun,Kwak, Young-Shin,Jeong, Jin-Hyun

scheme or table, p. 6588 - 6589 (2011/02/21)

A library of 2,3-disubstituted benzofuran scaffold was developed by using intramolecular Wittig olefination and Friedel-Crafts acylation.

Synthesis and preliminary characterization of a novel antiarrhythmic compound (KB130015) with an improved toxicity profile compared with amiodarone

Carlsson, Bo,Singh,Temciuc, Marcel,Nilsson, Stefan,Li, Yi-Lin,Mellin, Charlotta,Malm, Johan

, p. 623 - 630 (2007/10/03)

Recent developments in antiarrhythmic therapy have indicated that the best approach to pharmacologically controlling supraventricular arrhythmias and life-threatening ventricular tachyarrhythmias is by prolonging cardiac repolarization rather than by bloc

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