1113009-72-5

Basic information

• Product Name: acetic acid 1-{2-[1-acetoxy-3-(4-chloro-phenyl)-prop-2-ynyl]-phenyl}-3-(4-chloro-phenyl)-prop-2-ynyl ester
• Synonyms: acetic acid 1-{2-[1-acetoxy-3-(4-chloro-phenyl)-prop-2-ynyl]-phenyl}-3-(4-chloro-phenyl)-prop-2-ynyl ester
• CAS NO: 1113009-72-5
• Molecular Weight: 491.37
• Mol File: 1113009-72-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: acetic acid 1-{2-[1-acetoxy-3-(4-chloro-phenyl)-prop-2-ynyl]-phenyl}-3-(4-chloro-phenyl)-prop-2-ynyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: acetic acid 1-{2-[1-acetoxy-3-(4-chloro-phenyl)-prop-2-ynyl]-phenyl}-3-(4-chloro-phenyl)-prop-2-ynyl ester(1113009-72-5)
• EPA Substance Registry System: acetic acid 1-{2-[1-acetoxy-3-(4-chloro-phenyl)-prop-2-ynyl]-phenyl}-3-(4-chloro-phenyl)-prop-2-ynyl ester(1113009-72-5)

Safety Data

• Hazardous Substances Data: 1113009-72-5(Hazardous Substances Data)

Upstream product

• 942229-68-7 C₂₄H₁₆O₂Cl₂ 
• 75-36-5 acetyl chloride 

Downstream Products

• 1113009-90-7 (4-chloro-phenyl)-[3-(4-chloro-phenylethynyl)-1H-inden-2-yl]-methanone 
• 108-24-7 acetic anhydride 

Relevant articles and documents

Highly efficient Bronsted acid-catalyzed cycloisomerizations of alkynes bearing bis(acetoxy) groups to indenyl ketones

A Bronsted acid-catalyzed cycloisomerization of functionalized alkynes is described, which is assumed to be initiated through the formation of a benzylic cation intermediate. The reaction offers a highly efficient and straightforward route to indenyl ketones with a wide range of substituents under mild conditions.