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3-Methoxydibenzofuran is an organic compound that is classified as a furan derivative. It consists of a dibenzofuran core with a methoxy group attached to the aromatic ring. This chemical is commonly used as a building block for the synthesis of various pharmaceuticals and agrochemicals.

20357-71-5

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20357-71-5 Usage

Uses

Used in Pharmaceutical Industry:
3-Methoxydibenzofuran is used as a building block for the synthesis of various pharmaceuticals. Its unique chemical structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
3-Methoxydibenzofuran is also used as a building block for the synthesis of various agrochemicals. Its chemical properties make it a valuable component in the development of new pesticides and other agricultural chemicals.
Environmental and Health Effects:
3-Methoxydibenzofuran has been studied for its potential environmental and health effects, as it is found in trace amounts in some environmental samples such as soil and air. However, more research is needed to fully understand the properties and potential risks associated with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 20357-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,5 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20357-71:
(7*2)+(6*0)+(5*3)+(4*5)+(3*7)+(2*7)+(1*1)=85
85 % 10 = 5
So 20357-71-5 is a valid CAS Registry Number.

20357-71-5SDS

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 3-methoxy-dibenzo[b,d]furan

1.2 Other means of identification

Product number -
Other names 3-methoxydibenzofuran

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:20357-71-5 SDS

20357-71-5Downstream Products

20357-71-5Relevant academic research and scientific papers

Nickel-catalyzed intramolecular C-H arylation using aryl pivalates as electrophiles

Wang, Jiayi,Ferguson, Devin M.,Kalyani, Dipannita

, p. 5780 - 5790 (2013/07/19)

This paper describes a method for nickel catalyzed intramolecular C-H arylation using aryl pivalates as electrophiles. The transformation is efficient for the synthesis of diverse electronically and sterically differentiated dibenzofurans. Additionally, the method could be expanded toward the synthesis of carbazoles. Preliminary mechanistic studies of the transformation are also described.

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