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1,3-Cyclohexanediol, 2-(hydroxymethyl)-2-methyl-, (1S,3S)- (9CI)

Base Information Edit
  • Chemical Name:1,3-Cyclohexanediol, 2-(hydroxymethyl)-2-methyl-, (1S,3S)- (9CI)
  • CAS No.:619335-74-9
  • Molecular Formula:C8H16O3
  • Molecular Weight:160.213
  • Hs Code.:
  • Mol file:619335-74-9.mol
1,3-Cyclohexanediol, 2-(hydroxymethyl)-2-methyl-, (1S,3S)- (9CI)

Synonyms:1,3-Cyclohexanediol, 2-(hydroxymethyl)-2-methyl-, (1S,3S)- (9CI)

Suppliers and Price of 1,3-Cyclohexanediol, 2-(hydroxymethyl)-2-methyl-, (1S,3S)- (9CI)
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 1,3-Cyclohexanediol, 2-(hydroxymethyl)-2-methyl-, (1S,3S)- (9CI) Edit
Chemical Property:
  • PSA:60.69000 
  • LogP:-0.10930 
Purity/Quality:

99%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 1,3-Cyclohexanediol, 2-(hydroxymethyl)-2-methyl-, (1S,3S)- (9CI)

There total 12 articles about 1,3-Cyclohexanediol, 2-(hydroxymethyl)-2-methyl-, (1S,3S)- (9CI) 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 hydrogen; nickel; In methanol; at 20 ℃; for 10h;
DOI:10.1016/j.tetlet.2003.08.009
Guidance literature:
Multi-step reaction with 5 steps
1: 96 percent / LiAlH4 / diethyl ether / 0.25 h / 0 °C
2: 92 percent / NaH; TBAI / tetrahydrofuran; dimethylformamide / 12 h / 20 °C
3: 95 percent / HCl / tetrahydrofuran / 0.5 h / 20 °C
4: 91 percent / (R)-CBS; BH3*SMe2 / CH2Cl2 / 10 h / 30 °C
5: Raney Ni; H2 / methanol / 10 h / 20 °C / atmospheric pressure
With hydrogenchloride; lithium aluminium tetrahydride; dimethylsulfide borane complex; hydrogen; tetra-(n-butyl)ammonium iodide; nickel; sodium hydride; (R)-(+)-2-methyl-CBS-oxazaborolidine; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo050349a
Guidance literature:
Multi-step reaction with 3 steps
1: 95 percent / HCl / tetrahydrofuran / 0.5 h / 20 °C
2: 91 percent / (R)-CBS; BH3*SMe2 / CH2Cl2 / 10 h / 30 °C
3: Raney Ni; H2 / methanol / 10 h / 20 °C / atmospheric pressure
With hydrogenchloride; dimethylsulfide borane complex; hydrogen; nickel; (R)-(+)-2-methyl-CBS-oxazaborolidine; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1021/jo050349a
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