32730-13-5

Basic information

• Product Name: Naphtho[1,2-b]furan, 3-phenyl-
• CAS NO: 32730-13-5
• Molecular Formula: C18H12O
• Molecular Weight: 244.293
• Mol File: 32730-13-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Naphtho[1,2-b]furan, 3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Naphtho[1,2-b]furan, 3-phenyl-(32730-13-5)
• EPA Substance Registry System: Naphtho[1,2-b]furan, 3-phenyl-(32730-13-5)

Safety Data

• Hazardous Substances Data: 32730-13-5(Hazardous Substances Data)

Upstream product

• 90-15-3 α-naphthol 
• 70-11-1 α-bromoacetophenone 
• 70049-85-3 3-(4'-bromophenyl)naphtho-[1, 2-b]furan 
• 833485-56-6 (2-benzoyl-naphthalen-1-yloxy)-acetic acid ethyl ester 
• 21009-99-4 2-benzoyl-1-naphthol 
• 607-55-6 α-naphthyl benzoate 
• 14621-59-1 2-(naphthalen-1-yloxy)-1-phenylethanone 

Downstream Products

• 91388-10-2 acetyl-2 phenyl-3 naphto<1,2-b>furanne 
• 91388-09-9 formyl-2 phenyl-3 naphto<1,2-b>furanne 

Relevant articles and documents

TfOH-SiO2 as an efficient and recyclable catalyst for synthesis of 3-arylbenzofurans

A convenient process for the synthesis of 3-arylbenzofurans and their derivatives by 2-phenoxy-1-phenylethanones via TfOH-SiO2 catalyzed is developed. This method provides several advantages such as simple work-up procedure, simple post-treatme

Titanium tetrachloride promoted cyclodehydration of aryloxyketones: Facile synthesis of benzofurans and naphthofurans with high regioselectivity

An efficient and facile method for the synthesis of a broad series of benzofurans and naphthofurans is described. The direct intramolecular cyclodehydration of aryloxyketones in the presence of titanium tetrachloride affords the corresponding benzofurans and naphthofurans with good regioselectivity and yields.

Novel one-pot synthesis of 3-Phenylnaphtho[2,3-b]furan and 3-phenylbenzofurans under microwave irradiation and solvent-free conditions

A one-pot synthesis of functionalized benzofurans has been developed via O-alkylation, carbon-carbon coupling/cyclization, and dehydration/olefination tandem reactions from phenacyl bromide and phenols under microwave irradiation and solvent-free conditio