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1,3-Cyclohexanedimethanol

Base Information
  • Chemical Name:1,3-Cyclohexanedimethanol
  • CAS No.:3971-28-6
  • Molecular Formula:C8H16 O2
  • Molecular Weight:144.214
  • Hs Code.:
  • European Community (EC) Number:223-594-5
  • DSSTox Substance ID:DTXSID70871047
  • Nikkaji Number:J175.273A
  • Mol file:3971-28-6.mol
1,3-Cyclohexanedimethanol

Synonyms:1,3-Cyclohexanedimethanol;3971-28-6;[3-(hydroxymethyl)cyclohexyl]methanol;1,3-Bis(hydroxymethyl)cyclohexane;EINECS 223-594-5;UNII-30B29WCY1W;SCHEMBL44806;Cyclohexane-1,3-diyldimethanol;30B29WCY1W;DTXSID70871047;AKOS006281257;AB85743;((1R,3S)-cyclohexane-1,3-diyl)dimethanol

Suppliers and Price of 1,3-Cyclohexanedimethanol
Supply Marketing:
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
  • American Custom Chemicals Corporation
  • 1,3-CYCLOHEXANEDIMETHANOL 95.00%
  • 5MG
  • $ 495.48
Total 13 raw suppliers
Chemical Property of 1,3-Cyclohexanedimethanol
Chemical Property:
  • Vapor Pressure:0.000705mmHg at 25°C 
  • Refractive Index:1.4912 (estimate) 
  • Boiling Point:274°Cat760mmHg 
  • Flash Point:131.5°C 
  • PSA:40.46000 
  • Density:1.004g/cm3 
  • LogP:0.77740 
  • XLogP3:0.8
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:144.115029749
  • Heavy Atom Count:10
  • Complexity:83.3
Purity/Quality:

98%Min *data from raw suppliers

1,3-CYCLOHEXANEDIMETHANOL 95.00% *data from reagent suppliers

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

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1CC(CC(C1)CO)CO
Technology Process of 1,3-Cyclohexanedimethanol

There total 13 articles about 1,3-Cyclohexanedimethanol 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 lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1016/S0960-894X(96)00279-X
Guidance literature:
With lithium aluminium tetrahydride; aluminium trichloride; In diethyl ether; at 20 ℃; for 2h;
Guidance literature:
Multi-step reaction with 2 steps
1: sulfuric acid / 24 h / Reflux
2: lithium aluminium tetrahydride / diethyl ether / 20 °C / Inert atmosphere; Cooling with ice
With lithium aluminium tetrahydride; sulfuric acid; In diethyl ether;
DOI:10.1107/S0108270113015060
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