917571-19-8

Basic information

• Product Name: 1(3H)-Isobenzofuranone, 6-chloro-3-[5-(1,1-dimethylethyl)-2-furanyl]-
• CAS NO: 917571-19-8
• Molecular Formula: C16H15ClO3
• Molecular Weight: 290.746
• Mol File: 917571-19-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1(3H)-Isobenzofuranone, 6-chloro-3-[5-(1,1-dimethylethyl)-2-furanyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1(3H)-Isobenzofuranone, 6-chloro-3-[5-(1,1-dimethylethyl)-2-furanyl]-(917571-19-8)
• EPA Substance Registry System: 1(3H)-Isobenzofuranone, 6-chloro-3-[5-(1,1-dimethylethyl)-2-furanyl]-(917571-19-8)

Safety Data

• Hazardous Substances Data: 917571-19-8(Hazardous Substances Data)

Upstream product

• 7040-43-9 2-tert-butylfuran 
• 4506-45-0 5-chloro-ortho-formylbenzoic acid 

Downstream Products

• 1033596-06-3 5-chloro-2-[(5-tert-butyl-2-furyl)methy]benzoic acid 

Relevant articles and documents

Furan ring opening - Isocoumarine ring closure: A recyclization reaction of 2-carboxyaryldifurylmethanes

A general method for the synthesis of isocoumarine derivatives has been developed. Bis(5-R-2-furyl)methylbenzoic acids (R = methyl, ethyl) underwent recyclization and subsequent cyclization into tetracyclic isochromene-1-one derivatives under treatment with hydrogen chloride in methanol. It has been shown that intermediate 4-(5-R-furan-2-yl)-3-(3-oxo-3-R-propyl)-isochromene-1- ones can be obtained selectively by varying a concentration of the hydrogen chloride and reaction times. In the case of R = tert-butyl only corresponding 4-[5-(tert-butyl)-2-furyl]-3-(4,4-dimethyl-3-oxopentyl)-1-isochromenones were isolated regardless of the reaction conditions.