124957-36-4

Basic information

• Product Name: 2-(ACETOXY-PHENYL-METHYL)-ACRYLIC ACID METHYL ESTER
• Synonyms: 2-(ACETOXY-PHENYL-METHYL)-ACRYLIC ACID METHYL ESTER;Methyl 2-[(acetyloxy)(phenyl)methyl]acrylate
• CAS NO: 124957-36-4
• Molecular Formula: C₁₃H₁₄O₄
• Molecular Weight: 234.25
• Mol File: 124957-36-4.mol
• Article Data: 57

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(ACETOXY-PHENYL-METHYL)-ACRYLIC ACID METHYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(ACETOXY-PHENYL-METHYL)-ACRYLIC ACID METHYL ESTER(124957-36-4)
• EPA Substance Registry System: 2-(ACETOXY-PHENYL-METHYL)-ACRYLIC ACID METHYL ESTER(124957-36-4)

Safety Data

• Hazardous Substances Data: 124957-36-4(Hazardous Substances Data)

Usage

Molecular structure

2-(acetoxy-phenyl-methyl)-acrylic acid methyl ester is a chemical compound that contains a benzene ring with an acetoxy group and a methyl ester group attached to an acrylic acid chain.

Classification

It is a methyl ester derivative of acrylic acid.

Usage

The compound is commonly used in the field of organic chemistry as a building block in chemical synthesis, and in the production of pharmaceuticals, agrochemicals, and other fine chemicals.

Reactivity

The compound can undergo a range of reactions to produce a variety of organic compounds and is used as a reagent in various organic transformations.

Polymer synthesis

2-(ACETOXY-PHENYL-METHYL)-ACRYLIC ACID METHYL ESTER can also serve as a starting material for the synthesis of polymers and copolymers.

Upstream product

• 18020-59-2 methyl 3-hydroxy-2-methylidene-3-phenylpropionate 
• 108-24-7 acetic anhydride 
• 100-52-7 benzaldehyde 
• 75-36-5 acetyl chloride 
• 107270-46-2 [α-(methoxycarbonyl)vinyl]diisobutylaluminum 
• 64-19-7 acetic acid 
• 67-56-1 methanol 

Downstream Products

• 137104-41-7 methyl (E)-2-<<(4-methoxyphenyl)amino>methyl>-3-phenylprop-2-enoate 
• 137104-50-8 methyl 2-<α-<(4-methoxyphenyl)amino>benzyl>prop-2-enoate 
• 849777-68-0 4-acetyl-2-methylene-5-oxo-3-phenylhexanoic acid methyl ester 

Relevant articles and documents

Radical Cascade-Triggered Controlled Ring-Opening Polymerization of Macrocyclic Monomers

A strategy for the controlled radical ring-opening polymerization of macrocyclic monomers is reported. Key to this approach is an allyl alkylsulfone-based ring-opening trigger that can undergo a radical cascade reaction to extrude sulfur dioxide and gener

1,3-Dipolar Cycloadditions to Baylis-Hillman Adducts: Rationale for the Observed Diastereoselectivity

Diazomethane and benzonitrile oxide cycloadditions were performed on Baylis-Hillman adducts derived from methyl acrylate and aldehydes (β'-alkoxy-α,β-unsaturated esters).The reactions proceed in good chemical yields, and their stereochemical outcome can b

COMPOSITIONS AND METHODS FOR PROTEIN LABELING, MODIFICATION, ANALYSIS, AND TARGETED DELIVERY

The invention relates to chemically reactive and/or biologically active compounds, reagents and compositions thereof. More particularly, the invention provides novel reagents that are useful in chemical synthesis, functionalization, delivery, probing and/or analytical measurements of small molecule drugs, proteins, antibodies and other biomolecules. The invention provides novel biologically active agents useful as diagnostics or therapeutics, and related composition and methods of uses thereof.

A one-pot three-step multicomponent synthesis of functionalized allyl dithiocarbamates using Baylis–Hillman reaction

A one-pot, pseudo five-component, highly diastereoselective, and mild procedure for the synthesis of functionalized allyl dithiocarbamates is developed. The Baylis–Hillman (BH) reaction of aromatic (heteroaromatic) aldehydes and activated alkenes using DA