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Encyclopedia

Trichodiene

Base Information Edit
  • Chemical Name:Trichodiene
  • CAS No.:28624-60-4
  • Molecular Formula:C15H24
  • Molecular Weight:204.356
  • Hs Code.:
  • UNII:697ERP55B1
  • DSSTox Substance ID:DTXSID201318181
  • Nikkaji Number:J17.359B
  • Wikidata:Q27098264
  • Metabolomics Workbench ID:28278
  • ChEMBL ID:CHEMBL2251626
  • Mol file:28624-60-4.mol
Trichodiene

Synonyms:trichodiene

Suppliers and Price of Trichodiene
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 1 raw suppliers
Chemical Property of Trichodiene Edit
Chemical Property:
  • Vapor Pressure:0.0244mmHg at 25°C 
  • Boiling Point:256.7°C at 760 mmHg 
  • Flash Point:99.2°C 
  • PSA:0.00000 
  • Density:0.89g/cm3 
  • LogP:4.86930 
  • XLogP3:4.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:1
  • Exact Mass:204.187800766
  • Heavy Atom Count:15
  • Complexity:310
Purity/Quality:

>95% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CCC(CC1)(C)C2(CCCC2=C)C
  • Isomeric SMILES:CC1=CC[C@@](CC1)(C)[C@]2(CCCC2=C)C
Technology Process of Trichodiene

There total 18 articles about Trichodiene 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 Tris buffer pH 7.8; 2-hydroxyethanethiol; magnesium chloride; at 30 ℃; for 16h; Further byproducts given. Title compound not separated from byproducts; D98E mutant of recombinant F. sporotrichioides trichodiene synthase;
DOI:10.1021/ja961897w
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) LDA
2: LiAlH4 / diethyl ether / 12 h / 25 °C
3: 1.) n-BuLi, N,N,N',N'-tetramethylethylenediamine / 1.) dimethoxyethane, hexane, 0 deg C, 5 min, 2.) dimethoxyethane, hexane, RT, 1 h
4: Li, t-BuOH, ethylamine / 2 h / 0 °C
With lithium aluminium tetrahydride; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; lithium; ethylamine; tert-butyl alcohol; lithium diisopropyl amide; In diethyl ether;
DOI:10.1021/jo00373a032
Guidance literature:
Multi-step reaction with 5 steps
1: 81 percent / pyridine / 12 h / Ambient temperature
2: 1.) LDA
3: LiAlH4 / diethyl ether / 12 h / 25 °C
4: 1.) n-BuLi, N,N,N',N'-tetramethylethylenediamine / 1.) dimethoxyethane, hexane, 0 deg C, 5 min, 2.) dimethoxyethane, hexane, RT, 1 h
5: Li, t-BuOH, ethylamine / 2 h / 0 °C
With pyridine; lithium aluminium tetrahydride; n-butyllithium; N,N,N,N,-tetramethylethylenediamine; lithium; ethylamine; tert-butyl alcohol; lithium diisopropyl amide; In diethyl ether;
DOI:10.1021/jo00373a032
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