CAS 4208-49-5

2-Propen-1-yl 2-furancarboxylate

Description:

2-Propen-1-yl 2-furancarboxylate, also known as furfuryl acrylate, is an organic compound characterized by its ester functional group derived from the reaction of furfural and acrylic acid. It features a furan ring, which contributes to its aromatic properties, and an acrylate group that provides reactivity, particularly in polymerization processes. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is soluble in organic solvents and exhibits moderate volatility. The presence of the double bond in the acrylate moiety allows for participation in various chemical reactions, making it useful in applications such as coatings, adhesives, and as a monomer in the production of polymers. Additionally, 2-propen-1-yl 2-furancarboxylate can undergo free radical polymerization, which is advantageous in creating cross-linked networks. Safety considerations include handling it in well-ventilated areas and using appropriate personal protective equipment, as it may cause skin and eye irritation.

Formula: C₈H₈O₃

InChI: InChI=1S/C8H8O3/c1-2-5-11-8(9)7-4-3-6-10-7/h2-4,6H,1,5H2

InChI key: InChIKey=SJRQTHAMRUOPBJ-UHFFFAOYSA-N

SMILES: C(OCC=C)(=O)C1=CC=CO1

Synonyms:

• 2-Furancarboxylic acid, 2-propen-1-yl ester
• 2-Furancarboxylic acid, 2-propenyl ester
• 2-Furoic acid, allyl ester
• 2-Furoic acid, allyl ester (8CI)
• 2-Propen-1-yl 2-furancarboxylate
• 2-Propen-1-yl 2-furoate
• 2-Propen-1-yl furan-2-carboxylate
• 2-Propenyl 2-furancarboxylate
• Allyl 2-furancarboxylate
• Allyl 2-furoate
• Allyl furoate
• Allyl pyromucate
• Einecs 224-128-3
• FEMA No. 2030
• NSC 18604

Allyl furan-2-carboxylate

CAS: 4208-49-5

Formula: C₈H₈O₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 152.1473

Ref: IN-DA003NPI

Allyl Furan-2-Carboxylate

CAS: 4208-49-5

Allyl Furan-2-Carboxylate

Purity: 98%

Molecular weight: 152.15g/mol

Ref: 54-OR1029639

Allyl 2-furoate

CAS: 4208-49-5

Allyl 2-furoate is a non-volatile compound that has been shown to have insecticidal properties against lepidoptera. It binds to the fatty acid synthase enzyme of the target insect, which is essential for the production of fatty acids. This leads to a disruption in the synthesis of fats and proteins, causing death by starvation. Allyl 2-furoate also inhibits acetylcholinesterase and phosphodiesterase, which are enzymes that are important for neurotransmitter release and muscle contraction respectively. Allyl 2-furoate is soluble in solvents such as ether, chloroform, benzene, and ethyl acetate. Its molecular weight is 136.2 g/mol with a target tissue of tissues or cells that contain alkene groups (e.g., ovaries).

Formula: C₈H₈O₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 152.15 g/mol

Ref: 3D-FA70181

Allyl furan-2-carboxylate

CAS: 4208-49-5

Formula: C₈H₈O₃

Purity: 98%

Molecular weight: 152.149

Ref: 10-F546197