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2,2,5-Trimethylhex-4-enal

Base Information Edit
  • Chemical Name:2,2,5-Trimethylhex-4-enal
  • CAS No.:1000-30-2
  • Molecular Formula:C9H16 O
  • Molecular Weight:140.225
  • Hs Code.:2912190090
  • European Community (EC) Number:213-670-6
  • DSSTox Substance ID:DTXSID20142850
  • Nikkaji Number:J217.099J
  • Mol file:1000-30-2.mol
2,2,5-Trimethylhex-4-enal

Synonyms:2,2,5-Trimethylhex-4-enal;1000-30-2;4-Hexenal, 2,2,5-trimethyl-;2,2,5-trimethyl-4-hexenal;EINECS 213-670-6;2,2,5-trimethyl-hex-4-enal;SCHEMBL1114594;DTXSID20142850;2,2,5-trimethyl-4-hexen-1-al;AKOS022633932;EN300-368105;F2147-6390

Suppliers and Price of 2,2,5-Trimethylhex-4-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
Total 23 raw suppliers
Chemical Property of 2,2,5-Trimethylhex-4-enal Edit
Chemical Property:
  • Vapor Pressure:0.777mmHg at 25°C 
  • Boiling Point:183.3°Cat760mmHg 
  • Flash Point:57.5°C 
  • PSA:17.07000 
  • Density:0.835g/cm3 
  • LogP:2.56780 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:3
  • Exact Mass:140.120115130
  • Heavy Atom Count:10
  • Complexity:139
Purity/Quality:

99.0% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=CCC(C)(C)C=O)C
Technology Process of 2,2,5-Trimethylhex-4-enal

There total 11 articles about 2,2,5-Trimethylhex-4-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 sodium hydroxide; tetra-(n-butyl)ammonium iodide; In toluene; at 80 ℃; for 4.5h;
Guidance literature:
With oxalyl dichloride; dimethyl sulfoxide; triethylamine; In dichloromethane; at -78 - 20 ℃;
DOI:10.1021/ja0672932
Guidance literature:
Multistep reaction; (i) EtMgBr, (ii) /BRN= 1420778/;
DOI:10.1002/hlca.19780610531
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