1,3-Dimethylcyclopentanol

Base Information

• Chemical Name: 1,3-Dimethylcyclopentanol
• CAS No.: 19550-46-0
• Molecular Formula: C7H14 O
• Molecular Weight: 114.188
• Hs Code.: 2906199090
• DSSTox Substance ID: DTXSID80941326
• Nikkaji Number: J3.400.134K
• Mol file: 19550-46-0.mol

Synonyms:1,3-Dimethylcyclopentanol;19550-46-0;1,3-dimethylcyclopentan-1-ol;1,3-Dimethyl cyclopentanol;1.3-Dimethylcyclopentanol-1;Cyclopentanol, 1,3-dimethyl-;Dimehtyl cyclopentanol, 1,3-;Dimethyl cyclopentanol, 1,3-;1,3-Dimethylcyclopentane-1-ol;SCHEMBL2343536;DTXSID80941326;AKOS006271496;AS-82567;FT-0714541;E77662;EN300-693621

Chemical Property of 1,3-Dimethylcyclopentanol

Chemical Property:

• Vapor Pressure: 1.45mmHg at 25°C
• Boiling Point: 150.5°Cat760mmHg
• Flash Point: 54.4°C
• PSA: 20.23000
• Density: 0.92g/cm³
• LogP: 1.55740
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 114.104465066
• Heavy Atom Count: 8
• Complexity: 90.4

Purity/Quality:

99%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Chemical Classes: Other Classes -> Alcohols and Polyols, Other
• Canonical SMILES: CC1CCC(C1)(C)O

Technology Process of 1,3-Dimethylcyclopentanol

There total 8 articles about 1,3-Dimethylcyclopentanol 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:

Reference yield:

2,5-hexanedione (110-13-4) → 2,5-dimethyltetrahydrofuran (1003-38-9) + hexane-2,5-diol (2935-44-6) + 1,3-dimethylcyclopentan-1-ol (19550-46-0)

Guidance literature:

With acetonitrile(4′-phenyl-2,2′:6′,2”-terpyridine)(8-quinolinethiolate)ruthenium(II) triflate; hydrogen; In water; at 225 ℃; for 16h; under 41254.1 Torr; Autoclave;

DOI:10.1016/j.poly.2015.10.049

Reference yield:

2,5-hexanedione (110-13-4) → 2,5-dimethyltetrahydrofuran (1003-38-9) + 1,3-dimethylcyclopentan-1-ol (19550-46-0)

Guidance literature:

With [Ru(trifluoromethanesulfonate)(2,2′-bipyridine)(4′-phenyl-2,2′:6′,2”-terpyridine)](trifluoromethanesulfonate); hydrogen; In water; at 225 ℃; for 16h; under 41254.1 Torr; Autoclave;

DOI:10.1016/j.poly.2015.10.049

Reference yield:

2,5-dimethylfuran (625-86-5) → 2,5-dimethyltetrahydrofuran (1003-38-9) + hexane-2,5-diol (2935-44-6) + 1,3-dimethylcyclopentan-1-ol (19550-46-0) + 2,5-hexanedione (110-13-4)

Guidance literature:

With trifluorormethanesulfonic acid; acetonitrile(4′-phenyl-2,2′:6′,2”-terpyridine)(8-quinolinethiolate)ruthenium(II) triflate; hydrogen; In water; at 200 ℃; for 16h; under 41254.1 Torr; Autoclave;

DOI:10.1016/j.poly.2015.10.049

upstream raw materials:

cis-1,3-dimethylcyclopentane

2,5-hexanedione

2,5-dimethylfuran

Downstream raw materials:

1,4-dimethylcyclopentene

cis-1,3-dimethylcyclopentane

trans-1,3-dimethylcyclopentane

Refernces