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3-(8,11,14-Pentadecatrienyl)phenol

Base Information
  • Chemical Name:3-(8,11,14-Pentadecatrienyl)phenol
  • CAS No.:79353-39-2
  • Molecular Formula:C21H30O
  • Molecular Weight:298.469
  • Hs Code.:
  • Nikkaji Number:J167.346G,J489.558D
  • Metabolomics Workbench ID:46246
3-(8,11,14-Pentadecatrienyl)phenol

Synonyms:3-(8,11,14-Pentadecatrienyl)phenol;Anacardol IV;3-[(8E,11E)-pentadeca-8,11,14-trienyl]phenol;CHEBI:171704;3-(pentadeca-8,11,14-trienyl) phenol;3-(8z,11z)-8,11,14-Pentadecatrienyl-Phenol;3-[(8E,11E)-pentadeca-8,11,14-trien-1-yl]phenol

Suppliers and Price of 3-(8,11,14-Pentadecatrienyl)phenol
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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  • price
Total 7 raw suppliers
Chemical Property of 3-(8,11,14-Pentadecatrienyl)phenol
Chemical Property:
  • Vapor Pressure:7.49E-08mmHg at 25°C 
  • Boiling Point:425.8°Cat760mmHg 
  • Flash Point:192.3°C 
  • Density:0.941g/cm3 
  • XLogP3:7.6
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:12
  • Exact Mass:298.229665576
  • Heavy Atom Count:22
  • Complexity:316
Purity/Quality:

≥95% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C=CCC=CCC=CCCCCCCCC1=CC(=CC=C1)O
  • Isomeric SMILES:C=CC/C=C/C/C=C/CCCCCCCC1=CC(=CC=C1)O
Refernces

Antitumor principles from Ginkgo biloba L.

10.1248/cpb.35.3016

This research aimed to isolate and identify antitumor principles from Ginkgo biloba L., focusing on their effectiveness against Sarcoma 180 ascites in mice. The study successfully isolated seven long-chain phenols, among which anacardic acid (Ib), bilobol (IIa), and cardanol (IIIa) demonstrated significant antitumor activity, with effectiveness rated as (+++) for Ib, (++) for IIa, and (+++) for IIIa at a dosage of 40 mg/kg/day. The compounds were further purified using high-performance liquid chromatography (HPLC) and characterized through spectral data analysis, which included ultraviolet, infrared, nuclear magnetic resonance, and mass spectrometry. The study concluded that the antitumor activity against Sarcoma 180 ascites does not require the carboxyl group, in contrast to the antimicrobial activity which does.

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