Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

(E)-hexadec-11-enal

Base Information Edit
  • Chemical Name:(E)-hexadec-11-enal
  • CAS No.:57491-33-5
  • Molecular Formula:C16H30 O
  • Molecular Weight:238.414
  • Hs Code.:
  • European Community (EC) Number:260-765-3
  • DSSTox Substance ID:DTXSID601016280
  • Nikkaji Number:J296.713H,J60.913G
  • Metabolomics Workbench ID:3490
  • Mol file:57491-33-5.mol
(E)-hexadec-11-enal

Synonyms:11-Hexadecenal,(E)-; (E)-11-Hexadecenal

Suppliers and Price of (E)-hexadec-11-enal
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • (11E)-11-Hexadecenal
  • 25mg
  • $ 275.00
  • American Custom Chemicals Corporation
  • (E)-HEXADEC-11-ENAL 95.00%
  • 5MG
  • $ 501.59
Total 9 raw suppliers
Chemical Property of (E)-hexadec-11-enal Edit
Chemical Property:
  • Vapor Pressure:0.000253mmHg at 25°C 
  • Boiling Point:324°Cat760mmHg 
  • Flash Point:156.6°C 
  • PSA:17.07000 
  • Density:0.84g/cm3 
  • LogP:5.44260 
  • XLogP3:6.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:13
  • Exact Mass:238.229665576
  • Heavy Atom Count:17
  • Complexity:172
Purity/Quality:

98%,99%, *data from raw suppliers

(11E)-11-Hexadecenal *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCC=CCCCCCCCCCC=O
  • Isomeric SMILES:CCCC/C=C/CCCCCCCCCC=O
  • Uses (11E)-11-Hexadecenal is a monounsaturated 16 carbon aldehyde found in pheromones of insects.
Technology Process of (E)-hexadec-11-enal

There total 13 articles about (E)-hexadec-11-enal which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With oxalyl dichloride; dimethyl sulfoxide; In dichloromethane; at -60 ℃; for 0.25h;
DOI:10.1021/jo00376a043
Guidance literature:
11-hexadecene-1-ol; With oxalyl dichloride; dimethyl sulfoxide; In dichloromethane; at -78 ℃; for 0.25h;
With triethylamine; In dichloromethane; Overall yield = 95 %; Overall yield = 0.20 g;
Guidance literature:
Multi-step reaction with 3 steps
1: 1.) ThxBHCl*Me2S, 2.) KIPBH, 3.) NaOMe, 4.) AcOH
2: 97 percent / 20percent aq. NaOH / aq. ethanol / 0.5 h / Ambient temperature
3: 98 percent / oxalyl chloride, Me2SO / CH2Cl2 / 0.25 h / -60 °C
With sodium hydroxide; potassium tri(isopropoxy)borohydride; oxalyl dichloride; thexylchloroborane*methyl sulfide; sodium methylate; acetic acid; dimethyl sulfoxide; In ethanol; dichloromethane;
DOI:10.1021/jo00376a043
Post RFQ for Price