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6307-20-6

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6307-20-6 Usage

General Description

2,3,5-triphenylfuran is a chemical compound that belongs to the furan family, which is characterized by a heterocyclic structure containing a five-membered ring with four carbon atoms and one oxygen atom. The three phenyl groups attached to the furan ring make this compound a substituted derivative of furan. 2,3,5-triphenylfuran has been studied for its potential use in organic synthesis, particularly in the development of new materials for electronic devices and organic light-emitting diodes. It has also shown promise as a building block for the synthesis of novel organic compounds with potential pharmaceutical applications. Additionally, the compound is being investigated for its potential antimicrobial and antioxidant properties, making it a subject of interest in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 6307-20-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6307-20:
(6*6)+(5*3)+(4*0)+(3*7)+(2*2)+(1*0)=76
76 % 10 = 6
So 6307-20-6 is a valid CAS Registry Number.

6307-20-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5-triphenylfuran

1.2 Other means of identification

Product number -
Other names 2,3,5-triphenyl-furan

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:6307-20-6 SDS

6307-20-6Relevant articles and documents

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Sundholm,Smith

, p. 3459,3462 (1951)

-

Photoredox-Enabled Chromium-Catalyzed Alkene Diacylations

Liu, Jing,Lu, Liang-Qiu,Luo, Yixin,Zhao, Wei,Sun, Peng-Chao,Jin, Weiwei,Qi, Xiaotian,Cheng, Ying,Xiao, Wen-Jing

, p. 1879 - 1885 (2022/02/07)

Transition-metal-catalyzed cross-coupling reactions are a powerful tool to construct carbon-carbon bonds in modern synthetic chemistry. Chromium catalysis is much less developed compared with the widely used palladium and nickel catalysis. Herein, we repo

Visible-Light-Promoted Photocatalyst-Free Hydroacylation and Diacylation of Alkenes Tuned by NiCl2·DME

Zhao, Xinxin,Li, Bing,Xia, Wujiong

supporting information, p. 1056 - 1061 (2020/02/15)

Herein, we describe a visible light-promoted hydroacylation strategy that facilitates the preparation of ketones from alkenes and 4-acyl-1,4-dihydropyridines via an acyl radical addition and hydrogen atom transfer pathway under photocatalyst-free conditions. The efficiency was highlighted by wide substrate scope, good to high yields, successful scale-up experiments, and expedient preparation of highly functionalized ketone derivatives. In addition, this protocol allows for the synthesis of 1,4-dicarbonyl compounds through alkene diacylation in the presence of NiCl2·DME.

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