444107-43-1

Basic information

• Product Name: 2-(4-chlorobenzylidene)-4-methoxyfurano[3,2-f]benzofuran-3(2H)-one
• Synonyms: 2-(4-chlorobenzylidene)-4-methoxyfurano[3,2-f]benzofuran-3(2H)-one
• CAS NO: 444107-43-1
• Molecular Weight: 326.736
• Mol File: 444107-43-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(4-chlorobenzylidene)-4-methoxyfurano[3,2-f]benzofuran-3(2H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-chlorobenzylidene)-4-methoxyfurano[3,2-f]benzofuran-3(2H)-one(444107-43-1)
• EPA Substance Registry System: 2-(4-chlorobenzylidene)-4-methoxyfurano[3,2-f]benzofuran-3(2H)-one(444107-43-1)

Safety Data

• Hazardous Substances Data: 444107-43-1(Hazardous Substances Data)

Upstream product

• 484-27-5 5-acetyl-4-methoxybenzofuran-6-ol 
• 104-88-1 4-chlorobenzaldehyde 
• 444107-39-5 C₁₈H₁₃ClO₄ 
• 82-57-5 visnagin 

Relevant articles and documents

Celecoxib analogs bearing benzofuran moiety as cyclooxygenase-2 inhibitors: Design, synthesis and evaluation as potential anti-inflammatory agents

Novel series of celecoxib analogs endowed with benzofuran moiety 3a-e and 9a-d were synthesized and evaluated for COX-1/COX-2 inhibitory activity in vitro. The most potent and selective COX-2 inhibitors - compounds 3c, 3d, 3e, 9c and 9d - were assessed fo

Photochemical reaction of phenanthrenequinone with some new aurones derived from khellin and visnagin

Phenanthrenequinone 2 and aurones 5a-h are potentially capable of undergoing an interesting photochemical reaction leading to the formation of the adducts 6a-h. The structures of the 1,4-dioxine derivatives 6a-h were firmly established on the basis of analytical data and spectroscopic evidences.