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2-(furan-2-ylmethylidene)-1-benzofuran-3(2H)-one is a complex organic compound characterized by a benzofuran core, which is a fused ring system consisting of a benzene ring and a furan ring. The molecule features a furan-2-ylmethylidene group (a methylene bridged to a furan ring) at the 2-position and a ketone functional group at the 3-position, indicating the presence of a carbonyl group. This chemical structure endows the compound with specific electronic and steric properties, which can influence its reactivity, stability, and potential applications in various fields such as pharmaceuticals, materials science, or as a synthetic intermediate. The compound's unique arrangement of atoms and functional groups may also contribute to its distinct physical and chemical characteristics.

6622-21-5

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6622-21-5 Usage

Chemical structure

Contains a furan ring and a benzofuran ring, as well as a carbonyl group.

Classification

Organic compound.

Applications

Often used in research and pharmaceutical applications due to its potential biological activity.

Potential uses

May have applications in medicinal chemistry as a potential drug candidate or as a building block for the synthesis of other compounds.

Additional research

Its specific properties and potential uses would depend on further research and testing.

Check Digit Verification of cas no

The CAS Registry Mumber 6622-21-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6622-21:
(6*6)+(5*6)+(4*2)+(3*2)+(2*2)+(1*1)=85
85 % 10 = 5
So 6622-21-5 is a valid CAS Registry Number.

6622-21-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(furan-2-ylmethylidene)-1-benzofuran-3-one

1.2 Other means of identification

Product number -
Other names -

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:6622-21-5 SDS

6622-21-5Relevant academic research and scientific papers

2-Chlorophenyl-substituted benzofuro[3,2-b]pyridines with enhanced topoisomerase inhibitory activity: The role of the chlorine substituent

Thapa Magar, Til Bahadur,Kadayat, Tara Man,Lee, Hwa-Jong,Park, Seojeong,Bist, Ganesh,Shrestha, Aarajana,Kwon, Youngjoo,Lee, Eung-Seok

, p. 3279 - 3283 (2017/07/07)

A new series of 2-chloropheny-substituted benzofuro[3,2-b]pyridines were designed, synthesized, and evaluated for topoisomerase I and II inhibition and antiproliferative activity. Compounds 17–19, 23, 24, 26, and 27 exhibited excellent topo II inhibitory

A series of novel terpyridine-skeleton molecule derivants inhibit tumor growth and metastasis by targeting topoisomerases

Kwon, Han-Byeol,Park, Chanmi,Jeon, Kyung-Hwa,Lee, Eunyoung,Park, So-Eun,Jun, Kyu-Yeon,Kadayat, Tara Man,Thapa, Pritam,Karki, Radha,Na, Younghwa,Park, Mi Sun,Rho, Seung Bae,Lee, Eung-Seok,Kwon, Youngjoo

, p. 1100 - 1122 (2015/03/04)

A series of novel terpyridine-skeleton molecules containing conformational rigidity, 14 containing benzo[4,5]furo[3,2-b]pyridine core and 15 comprising chromeno[4,3-b]pyridine core, were synthesized, and their biological activities were evaluated. 3-(4-Ph

2,4-Diaryl benzofuro[3,2-b]pyridine derivatives: Design, synthesis, and evaluation of topoisomerase inhibitory activity and cytotoxicity

Thapa, Pritam,Jahng, Yurngdong,Park, Pil-Hoon,Jee, Jun-Goo,Kwon, Youngjoo,Lee, Eung-Seok

, p. 3073 - 3082 (2014/01/06)

Designed and synthesized twenty-four 2,4-diaryl benzofuro[3,2-b]pyridine derivatives were evaluated for topoisomerase I and II inhibitory activities as well as cytotoxicities against several human cancer cell lines. Various aryl groups such as phenyl, 2-

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