Cinnamyl butyrate

CAS: 103-61-7

Ref. 3D-FC69788

Produktinformation

• Name: Cinnamyl butyrate
• Synonyme: (2E)-3-phenylprop-2-en-1-yl butanoate, 3-Phenyl-2-propen-1-yl butanoate, 3-Phenyl-2-propen-1-yl butyrate, 3-Phenyl-2-propenyl butanoate, 3-Phenylallyl butyrate, 3-Phenylprop-2-En-1-Yl Butanoate, 3-Phenylprop-2-enyl butanoate, Ai3-02461, Brn 3200585, Butanoic acid, 3-phenyl-2-propen-1-yl ester, Butanoic acid, 3-phenyl-2-propenyl ester, Butynoic acid, 3-phenyl-2-propenyl ester, Butyric acid, cinnamyl ester, Cinnamyl alcohol, butyrate, Cinnamyl butanoate, Cinnamyl n-butyrate, FEMA No. 2296, Fema 2296, Nsc 30528, Phenylpropenyl n-butyrate, 2-06-00-00527 (Beilstein Handbook Reference), Cinnamyl butyrate

Beschreibung

Cinnamyl butyrate is a chemical compound that belongs to the class of diphenyl ethers. It has been shown to reduce plasma glucose levels in mice by inhibiting fatty acid synthesis and stimulating glucose uptake into cells. Cinnamyl butyrate also acts as a cross-linking agent, which enhances the stability of polymers by forming covalent bonds between reactive groups. The surface methodology used for this study was a surface science technique called atomic force microscopy (AFM). This method can be used to measure the thickness of the film, or the diameter of the particles. The AFM images showed that cinnamyl butyrate formed a thin film that was uniform over large areas.

Cinnamyl butyrate inhibited glucose absorption in vitro, which may be due to its ability to inhibit fatty acid synthesis and stimulate glucose uptake into cells. Cinnamyl butyrate also acts as a cross-linking agent, which enhances

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 204.26 g/mol
• Formel: C₁₃H₁₆O₂
• Reinheit: Min. 95%
• Farbe/Form: Clear Liquid
• InChl: InChI=1S/C13H16O2/c1-2-7-13(14)15-11-6-10-12-8-4-3-5-9-12/h3-6,8-10H,2,7,11H2,1H3/b10-6+
• InChI Key: InChIKey=YZYPQKZWNXANRB-UXBLZVDNSA-N
• SMILES: CCCC(=O)OC/C=C/c1ccccc1