53598-05-3

Usage

Uses

Used in Polymer Production:
2-Propenoic acid, 3-(3-chlorophenyl)-2-methylis used as a monomer in the production of polymers. Its unique chemical structure allows it to be copolymerized with other monomers, resulting in polymers with specific properties and applications.
Used in Organic Synthesis:
2-Propenoic acid, 3-(3-chlorophenyl)-2-methylis used as a building block in organic synthesis. Its reactivity and functional groups make it a versatile compound for the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Chemical Research:
2-Propenoic acid, 3-(3-chlorophenyl)-2-methylis also used in chemical research as a model compound to study the properties and reactions of acrylic acid derivatives. This helps researchers to understand the behavior of similar compounds and develop new synthetic routes and applications.

Upstream product

• 123-62-6 propionic acid anhydride 
• 587-04-2 m-Chlorobenzaldehyde 
• 802294-64-0 propionic acid 
• 7796-34-1 tripropionyloxyborane 

Downstream Products

• 91445-89-5 3-(3-Chlor-phenyl)-2,3-dibrom-2-methyl-propionsaeure 
• 43136-84-1 1-chloro-3-(prop-1-yn-1-yl)benzene 
• 66735-00-0 3-(3-chloro-phenyl)-2-methyl-propionic acid 

Relevant academic research and scientific papers

Sodium tetraborate-dibenzo-18-crown ether-6 complex as reagent in the synthesis of cinnamic acids from aromatic aldehydes and aliphatic carboxylic acids

Cinnamic acids have been prepared in 74-81% yields by a new synthesis from aromatic aldehydes and aliphatic carboxylic acids in the presence of anhydrous sodium tetraborate-dibenzo-18-crown ether-6 complex as reagent, 4-dimethylaminopyridine as activating agent, pyridine as base, and N-methyl-2-pyrolidinone as solvent, at reflux (180-190°C) for 10-12 hours.

A novel approach in cinnamic acid synthesis: Direct synthesis of cinnamic acids from aromatic aldehydes and aliphatic carboxylic acids in the presence of boron tribromide

Cinnamic acids have been prepared in moderate to high yields by a new direct synthesis using aromatic aldehydes and aliphatic carboxylic acids, in the presence of boron tribromide as reagent, 4-dimethylaminopyridine (4-DMAP) and pyridine (Py) as bases and N-methyl-2-pyrolidinone (NMP) as solvent, at reflux (180-190°C) for 8-12 hours.

New boron reagents for designed organic synthesis. 2 cinnamic acids synthesis in the presence of sodium tetramethoxyborate-lithium chloride

Cinnamic acids were prepared in good to high yields by Perkin reaction between aromatic aldehydes and aliphatic anhydrides in the presence of a boron compound, namely sodium tetramethoxyborate-lithium chloride, as a novel catalyst for this synthesis and N-methyl-pyrrolidin-2-one (NMP) as a solvent, at reflux (170-180°C) for 9-12 hours.

A new direct synthesis of cinnamic acids from aromatic aldehydes and aliphatic carboxylic acids in the presence of sodium borohydride

Cinnamic acids have been prepared in 59-86% yields by a new direct synthesis from aromatic aldehydes and aliphatic carboxylic acids in the presence of sodium borohydride and N-methyl-2-pyrrolidinone (NMP) as solvent, at reflux (185-190°C), for 9-12 hours. Without sodium borohydride, this reaction is not possible.