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(S)-2-Methyl-1-penten-3-ol

Base Information Edit
  • Chemical Name:(S)-2-Methyl-1-penten-3-ol
  • CAS No.:98168-21-9
  • Molecular Formula:C6H12O
  • Molecular Weight:100.161
  • Hs Code.:
  • UNII:F4K5QX6BR3
  • Nikkaji Number:J792.068G
  • Mol file:98168-21-9.mol
(S)-2-Methyl-1-penten-3-ol

Synonyms:F4K5QX6BR3;(-)-2-Methyl-1-penten-3-ol;(3S)-2-Methyl-1-penten-3-ol;2-Methyl-1-penten-3-ol, (S)-;2-Methyl-1-penten-3-ol, (-)-;UNII-F4K5QX6BR3;1-Penten-3-ol, 2-methyl-, (3S)-;98168-21-9;(S)-2-Methyl-1-penten-3-ol

Suppliers and Price of (S)-2-Methyl-1-penten-3-ol
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 0 raw suppliers
Chemical Property of (S)-2-Methyl-1-penten-3-ol Edit
Chemical Property:
  • PSA:20.23000 
  • LogP:1.33340 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:2
  • Exact Mass:100.088815002
  • Heavy Atom Count:7
  • Complexity:66.6
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCC(C(=C)C)O
  • Isomeric SMILES:CC[C@@H](C(=C)C)O
Technology Process of (S)-2-Methyl-1-penten-3-ol

There total 5 articles about (S)-2-Methyl-1-penten-3-ol 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 (1R,2S)-(+)-1-cyclohexyl-2-phenyl-2-(N-morpholino)ethanol; In hexane; toluene; at 20 ℃; for 3h; Title compound not separated from byproducts.;
DOI:10.1021/ol0259488
Guidance literature:
With naphthalene; (R)-1-(3-azabicyclo<3.2.2>nonan-3-yl)-3,3-dimethylbutan-2-ol; In hexane; at -10 ℃; for 24h; Yield given. Yields of byproduct given;
Guidance literature:
2-methylpropenal; ethylmagnesium bromide; In diethyl ether;
With titanium(IV) isopropylate; tert.-butylhydroperoxide; L-(+)-diisopropyl tartrate; 4 A molecular sieve; In dichloromethane; at -20 ℃; Title compound not separated from byproducts;
DOI:10.1055/s-2002-25364
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