Furfuryl acrylate

Base Information

• Chemical Name: Furfuryl acrylate
• CAS No.: 10525-17-4
• Molecular Formula: C8H8 O3
• Molecular Weight: 152.15
• Hs Code.: 2932190090
• European Community (EC) Number: 234-078-4
• NSC Number: 24158
• DSSTox Substance ID: DTXSID70147032
• Nikkaji Number: J212.456D
• Wikidata: Q83011952
• Mol file: 10525-17-4.mol

Synonyms:Furfuryl acrylate;10525-17-4;furan-2-ylmethyl prop-2-enoate;furan-2-ylmethyl acrylate;EINECS 234-078-4;AI3-03204;NSC24158;SCHEMBL397704;DTXSID70147032;Propenoic acid 2-furanylmethyl ester;MFCD00080516;NSC 24158;NSC-24158;AKOS006344462;FT-0691691

Chemical Property of Furfuryl acrylate

Chemical Property:

• Vapor Pressure: 0.387mmHg at 25°C
• Boiling Point: 197°Cat760mmHg
• Flash Point: 73°C
• PSA: 39.44000
• Density: 1.113g/cm³
• LogP: 1.50880
• XLogP3: 1.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 152.047344113
• Heavy Atom Count: 11
• Complexity: 153

Purity/Quality:

99% ^*data from raw suppliers

FURFURYL ACRYLATE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C=CC(=O)OCC1=CC=CO1

Technology Process of Furfuryl acrylate

There total 7 articles about Furfuryl 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: 94.0%

(2-furyl)methyl alcohol (98-00-0,25212-86-6,93793-62-5) + acryloyl chloride (814-68-6,25189-84-8) → furfuryl acrylate (10525-17-4)

Guidance literature:

With triethylamine; In dichloromethane; at 0 ℃; for 2h;

DOI:10.1002/anie.202009001

Reference yield: 84.5%

(2-furyl)methyl alcohol (98-00-0,25212-86-6,93793-62-5) + tert-butylmethyl ether-hexane + acryloyl chloride (814-68-6,25189-84-8) → furfuryl acrylate (10525-17-4)

Guidance literature:

With triethylamine; In tetrahydrofuran;

Reference yield: 70.0%

2-Chloromethylfuran (617-88-9) + sodium 2-propenoate (7446-81-3) → furfuryl acrylate (10525-17-4)

Guidance literature:

N-benzyl-N,N,N-triethylammonium chloride; In diethyl ether; at 25 - 30 ℃; for 10h;

DOI:10.1007/BF00497206

upstream raw materials:

(2-furyl)methyl alcohol

N-Phenyl-2-naphthylamine

acrylic acid methyl ester

2-Chloromethylfuran