112372

Ethyl cinnamate

99%

• Synonym(s): 3-Phenyl-2-propenoic acid ethyl ester, Ethyl 3-phenyl-2-propenoate, NSC 6773
• Linear Formula: C₆H₅CH=CHCOOC₂H₅
• CAS Number: 103-36-6
• Molecular Weight: 176.21
• Beilstein: 775541
• EC Number: 203-104-6
• MDL number: MFCD00009189
• UNSPSC Code: 12352100
• PubChem Substance ID: 24847091
• NACRES: NA.22

Properties

• Quality Level: 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.)
• 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

Description

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

Safety Information

• Storage Class Code: 10 - Combustible liquids
• WGK: WGK 1
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves