904328-01-4

Basic information

• Product Name: 5,5'-((4-bromo-2-nitrophenyl)methylene)bis(2-methylfuran)
• Synonyms: 5,5'-((4-bromo-2-nitrophenyl)methylene)bis(2-methylfuran)
• CAS NO: 904328-01-4
• Molecular Weight: 376.206
• Mol File: 904328-01-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5,5'-((4-bromo-2-nitrophenyl)methylene)bis(2-methylfuran)(CAS DataBase Reference)
• NIST Chemistry Reference: 5,5'-((4-bromo-2-nitrophenyl)methylene)bis(2-methylfuran)(904328-01-4)
• EPA Substance Registry System: 5,5'-((4-bromo-2-nitrophenyl)methylene)bis(2-methylfuran)(904328-01-4)

Safety Data

• Hazardous Substances Data: 904328-01-4(Hazardous Substances Data)

Upstream product

• 534-22-5 2-methylfuran 
• 5551-12-2 4-bromo-2-nitrobenzaldehyde 

Downstream Products

• 902136-42-9 2-acetylamino-4-bromophenylbis(5-methylfur-2-yl)methane 
• 902136-44-1 2-[bis-(5-methyl-furan-2-yl)-methyl]-5-bromo-phenylamine 

Relevant articles and documents

Reduction of bis(5-alkyl-2-furyl)(2-nitroaryl)methane with aqueous titanium trichloride solution

In this article, we introduces a new method for the synthesis of substituted indole by reductive recyclization of bis(5-alkyl-2-furyl)(2-nitroaryl)methane. Bis(5-alkyl-2-furyl)(2-nitroaryl)methane undergo reduction to provide indole or aniline. In the pro

Furan ring opening-indole ring closure: Synthesis of furo[2′, 3′:3,4]-cycloheota[1,2-b]indolium chlorides

A new synthetic approach to furo[2′,3′:3,4]cyclohepta[1,2-b] indolium chlorides is elaborated starting from 2-acetylaminoaryldifurylmethanes or 2-aminoaryldifurylmethanes under treatment with methanolic HCl solution. The reaction proceeds in three steps: recyclization, intramolecular cyclization, and disproportionation. In this case the furan ring takes part in building up both pyrrole and seven-membered rings. The same salts can be obtained directly from 2-acetylaminobenzaldehydes and 2-methylfuran under similar conditions without isolation of corresponding 2-acetylaminoaryldifurylmethanes.