Acrylate

Base Information

• Chemical Name: Acrylate
• CAS No.: 10344-93-1
• Molecular Formula: C₃H₃O₂
• Molecular Weight: 71.0556
• DSSTox Substance ID: DTXSID90145858
• Nikkaji Number: J215.982A
• Wikidata: Q27104395
• Mol file: 10344-93-1.mol

Synonyms:2-propenoic acid;acrylate;acrylic acid;acrylic acid, aluminum salt;acrylic acid, ammonium salt;acrylic acid, Ca (2:1) salt;acrylic acid, Ca (2:1) salt, dihydrate;acrylic acid, cobalt (2+) salt;acrylic acid, Fe (3+) salt;acrylic acid, magnesium salt;acrylic acid, potassium salt;acrylic acid, silver salt;acrylic acid, sodium salt;acrylic acid, zinc salt;Hystoacril;magnesium acrylate;vinylformic acid

Chemical Property of Acrylate

Chemical Property:

• Vapor Pressure: 3.42mmHg at 25°C
• Boiling Point: 141°Cat760mmHg
• Flash Point: 61.6°C
• PSA: 40.13000
• Density: g/cm³
• LogP: -1.07770
• XLogP3: 1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 71.013304334
• Heavy Atom Count: 5
• Complexity: 50.4

Purity/Quality:

98%,99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CC(=O)[O-]

Technology Process of Acrylate

There total 2 articles about Acrylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ acrylate (10344-93-1)

Guidance literature:

entspr. Komplex, Abbau;

DOI:10.1021/ja00843a011

Reference yield:

→ Acrylic acid anion (10344-93-1)

Guidance literature:

aus Acrylicsaeure durch γ-Bestrahlung;

DOI:10.1080/00268977300101841

Refernces

Facile generation of vicinal bromoazides from olefins using TMSN₃ and TsNBr₂ without any catalyst

10.1016/j.tetlet.2009.06.059

The research aimed to develop an efficient method for the synthesis of vicinal bromoazides directly from olefins using N,N-dibromo-p-toluenesulfonamide (TsNBr2) as the bromine source and trimethylsilyl azide (TMSN3) as the azide source, without the need for any catalyst. The study concluded that this method is extremely rapid and efficient, applicable to various olefins such as cinnamates, chalcone, styrenes, and acrylates, yielding the corresponding 1,2-bromoazides in excellent yields. The reaction is particularly effective for α,β-unsaturated carbonyl compounds, which are known to be challenging for such transformations. However, the reaction was found to be less effective for aliphatic alkenes like cyclohexene and 1-octene. The procedure is performed at room temperature in acetonitrile as the solvent, and the reaction is instantaneous, highlighting its ease of performance.

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