112372

Ethyl cinnamate

99%

• Synonyma: 3-Phenyl-2-propenoic acid ethyl ester, Ethyl 3-phenyl-2-propenoate, NSC 6773
• Lineární vzorec: C₆H₅CH=CHCOOC₂H₅
• Číslo CAS: 103-36-6
• Molekulová hmotnost: 176.21
• UNSPSC Code: 12352100
• NACRES: NA.22
• PubChem Substance ID: 24847091
• EC Number: 203-104-6
• Beilstein/REAXYS Number: 775541
• MDL number: MFCD00009189
• Assay: 99%

Vlastnosti

• Quality Segment: 100
• assay: 99%
• impurities: may contain alpha-tocopherol (synthetic)
• refractive index: n20/D 1.558 (lit.)
• bp: 271 °C (lit.)
• mp: 6-8 °C (lit.)
• density: 1.049 g/mL at 20 °C (lit.)
• functional group: ester, phenyl
• storage temp.: 2-8°C
• SMILES string: CCOC(=O)\C=C\c1ccccc1
• InChI: 1S/C11H12O2/c1-2-13-11(12)9-8-10-6-4-3-5-7-10/h3-9H,2H2,1H3/b9-8+
• InChI key: KBEBGUQPQBELIU-CMDGGOBGSA-N

Popis

Application

• Antimicrobial and antiproliferative effects: Essential oils including Ethyl cinnamate derived from Zingiberaceae family show promising antimicrobial and antiproliferative properties, suggesting their potential application in oral healthcare products. This study provides insight into the utilization of natural products for medical and pharmaceutical applications (Amil et al., 2024).
• Biodistribution and cellular interactions in medical research: Ethyl cinnamate could be investigated for its role in enhancing the permeability and imaging contrast in studies like those investigating the biodistribution of intravenously delivered mesenchymal stromal cells. Such applications could improve understanding in cellular therapies and regenerative medicine (Pichardo et al., 2022).

Biochem/physiol Actions

Ethyl cinnamate inhibits the growth of Chlorella pyrenoidosa.

Other Notes

2024 CiteAb Award Winner for Supplier Succeeding in Parkinson′s Research

Bezpečnostní informace

• Skladovací třída: 10 - Combustible liquids
• wgk: WGK 1
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)