857764-98-8

Basic information

• Product Name: Benzenepropanoyl chloride, b-chloro-
• CAS NO: 857764-98-8
• Molecular Formula: C9H8Cl2O
• Molecular Weight: 203.068
• Mol File: 857764-98-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenepropanoyl chloride, b-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoyl chloride, b-chloro-(857764-98-8)
• EPA Substance Registry System: Benzenepropanoyl chloride, b-chloro-(857764-98-8)

Safety Data

• Hazardous Substances Data: 857764-98-8(Hazardous Substances Data)

Upstream product

• 3480-87-3 3-hydroxy-3-phenylpropanoic acid 
• 100-52-7 benzaldehyde 
• 100-42-5 styrene 
• 75-44-5 phosgene 
• 15463-91-9 3-bromo-3-phenylpropionic acid 

Downstream Products

• 60786-21-2 3-chloro-3-phenylpropanoic acid 
• 6750-98-7 (E)-N-cyclohexylcinnamamide 
• 86449-82-3 1-cyclohexyl-4-phenylazetidinone 
• 13474-22-1 1,4-diphenyl-azetidin-2-one 
• 480-90-0 1H-inden-1-one 
• 408504-93-8 phenyl 3-chloro-3-phenylpropanamide 

Relevant articles and documents

Indenone synthesis. Improved synthetic protocol and effect of substitution on the intramolecular Friedel-Crafts acylation

An improved protocol for the construction of substituted indenones is presented. Also the effect of substitution on the intramolecular Friedel-Crafts acylation was noted. Specifically, if there is no substitution at the 2-position of the indenone poor yields of cyclized material were obtained, if at all, while the substitution of a methyl or ethyl group greatly improved the yield of cyclized material. Placement of a large group (e. g., benzyl) resulted in a diminuation of the improved yield. The new synthetic procedure could, in principle, allow for the construction of 2,3-disubstituted indenones. One example of this reaction mode was presented.