137338-08-0

Usage

Structure

Benzene derivative with an ethynyl group (-C≡CH) and an octyloxy group (-OC8H17) attached to its carbon atoms

Industrial Applications

Used as a building block in the synthesis of more complex organic molecules

Research and Development

Utilized as a reagent in chemical reactions

Fields of Application

Organic chemistry, pharmacology, and materials science

Safety Precautions

Proper handling and safety measures should be observed to prevent adverse effects on human health and the environment

InChI:InChI=1/C9H5FO/c1-2-7-4-3-5-9(10)8(7)6-11/h1,3-6H

Upstream product

• 608515-45-3 2-fluoro-6-(2-(trimethylsilyl)ethynyl)benzaldehyde 
• 360575-28-6 2-bromo-6-fluorobenzaldehyde 

Downstream Products

• 1638606-74-2 C₁₂H₉F 
• 1638606-37-7 C₁₉H₁₆FN₃O₂S 

Relevant academic research and scientific papers

Palladium-Catalyzed Aminomethylative Oppolzer-Type Cyclization of Enynes: Access to Aminomethylated Benzofulvenes

A novel palladium-catalyzed Oppolzer-type cyclization reaction aided by the aminomethyl cyclopalladated complex has been developed, which provides rapid access to functionalized benzofulvenes with excellent stereoselectivity. The corresponding products can undergo Diels–Alder reaction with maleimides, providing a series of complex polycyclic compounds with excellent regio- and stereoselectivities.

Palladium-catalyzed chemoselective aminomethylative cyclization and aromatizing allylic amination: Access to functionalized naphthalenes

A palladium-catalyzed chemoselective aminomethylative cyclization and aromatizing allylic amination of enyne-tethered allylic alcohols with aminals is described. Under the reaction conditions, the cationic vinyl allylpalladium species undergoes selective migratory insertion of alkenes rather than reductive elimination with nucleophiles. This strategy provides an efficient and unique approach to the construction of functionalized naphthalenes, which are important building blocks in synthetic organic chemistry. Mechanistic studies have revealed that the selective sequential migratory insertion of enyne and alkene is crucial for the cyclization.