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Methanone, (4-bromophenyl)[5-(4-bromophenyl)-3-(4-methoxyphenyl)-2-furanyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

219920-63-5

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219920-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219920-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,9,2 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 219920-63:
(8*2)+(7*1)+(6*9)+(5*9)+(4*2)+(3*0)+(2*6)+(1*3)=145
145 % 10 = 5
So 219920-63-5 is a valid CAS Registry Number.

219920-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-Bromobenzoyl)-5-(4-bromophenyl)-3-(4-methoxyphenyl)furan

1.2 Other means of identification

Product number -
Other names (4-Bromo-phenyl)-[5-(4-bromo-phenyl)-3-(4-methoxy-phenyl)-furan-2-yl]-methanone

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:219920-63-5 SDS

219920-63-5Downstream Products

219920-63-5Relevant academic research and scientific papers

Improved synthesis of pyrylium salts leading to 2,4-disubstituted diarylfurans via novel mechanism

Bello, Angélica M.,Kotra, Lakshmi P.

, p. 9271 - 9274 (2007/10/03)

Improved synthesis of pyrylium salts from either substituted benzoic acids or their methyl esters, and substituted acetophenone is reported en route to the synthesis of 2,4-diarylfurans. The mechanism involved in the formation of the pyrylium salt using t

A convenient synthesis of 2-aroyl-3,5-diarylfuran under microwave irradiation

Wang, Jin-Xian,Shi, Xiao-Ning,Zhao, Lian-Biao

, p. 586 - 587 (2007/10/03)

A simple, rapid and efficient method for the synthesis of 2-aroyl-3,5-diarylfuran under microwave irradiation is described. The effect of microwave irradiation power, times and solvent on the reaction is investigated.

A convenient regioselective synthesis of 2,4-diarylfurans

Francesconi, Iris,Patel, Alpa,Boykin, David W.

, p. 61 - 63 (2007/10/03)

A facile three step process, under mild conditions, for the synthesis of 2,4-diarylfurans with the same or different substituents on the two aryl rings, starting from benzaldehydes and acetophenones, employing Haller-Bauer type cleavage of 2-aroyl-3,5-diarylfurans is described.

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