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Usage

Uses

Used in Chemical and Pharmaceutical Industries:
2-Propenal, 3-(2-chlorophenyl)-2-Methylis used as a chemical intermediate for the production of various chemicals and pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of a range of compounds, contributing to the development of new drugs and chemical products.
Used as a Flavoring Agent in Food Industry:
In the food industry, 2-Propenal, 3-(2-chlorophenyl)-2-Methylis employed as a flavoring agent to impart specific taste profiles to food products. Its almond-like odor makes it suitable for enhancing the flavor of certain foods, adding a distinct and desirable quality to the final product.

Upstream product

• 78-84-2 isobutyraldehyde 
• 108-90-7 chlorobenzene 
• 89-98-5 2-chloro-benzaldehyde 
• 123-38-6 propionaldehyde 

Relevant academic research and scientific papers

Tetraalkylammonium and 1,3-dialkylimidazolium salts with fluorinated anions as recoverable phase-transfer catalysts in solid base-promoted cross-aldol condensations

Tetraalkylammonium and 1,3-dialkylimidazolium tetrafluoroborates and hexafluorophosphates were employed for the first time as recoverable phase-transfer catalysts in multiphase reactions of CH-acids, in particular in solid base-pro-moted cross-aldol condensations. The catalysts retained their catalytic activity over several reaction cycles.

Dehydrogenative β-Arylation of Saturated Aldehydes Using Transient Directing Groups

An unprecedented cross-dehydrogenative-coupling (CDC) reaction of saturated aldehyde β-C-H with arenes to form cinnamaldehydes via the cleavages of four C-H bonds has been developed. The reaction possesses complete E-stereoselectivity for the C=C double bond. The protocol is featured by atom and step economy, mild reaction conditions, and convenient operation.

Copper-Catalyzed Stereospecific Hydroboration of Internal Allylic Alcohols

An effective Cu-catalyzed stereospecific hydroboration of aliphatic and aromatic 1,1,2-trisubstituted internal allylic alcohols has been reported. This reaction proceeds via a silyl ether transient protection of allylic alcohols and subsequent stereospecific hydroboration. Followed by an oxidative workup, an array of acyclic, cyclic, and heterocyclic 1,3-diols was synthesized in good to excellent yields with good functional group tolerance and excellent diastereomeric ratios (> 20:1).