Cyclodecanol

Base Information

• Chemical Name: Cyclodecanol
• CAS No.: 1502-05-2
• Molecular Formula: C10H20O
• Molecular Weight: 156.268
• Hs Code.: 2906199090
• NSC Number: 88148
• UNII: DPG8P5THD7
• DSSTox Substance ID: DTXSID6061737
• Nikkaji Number: J80.211E
• Wikidata: Q20054511
• Mol file: 1502-05-2.mol

Synonyms:CYCLODECANOL;1502-05-2;Cyclodecyl alcohol;DPG8P5THD7;NSC 88148;NSC-88148;UNII-DPG8P5THD7;SCHEMBL290420;DTXSID6061737;NSC88148;CCG-40528;MFCD00039582;AKOS006274818;FT-0624161;J-008669;Q20054511

Chemical Property of Cyclodecanol

Chemical Property:

• Vapor Pressure: 0.00535mmHg at 25°C
• Melting Point: 40.5°C
• Refractive Index: 1.4926 (estimate)
• Boiling Point: 243.7°C at 760 mmHg
• PKA: 15.58±0.20(Predicted)
• Flash Point: 100.1°C
• PSA: 20.23000
• Density: 0.896g/cm³
• LogP: 2.87180
• XLogP3: 2.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 156.151415257
• Heavy Atom Count: 11
• Complexity: 80.9

Purity/Quality:

99% ^*data from raw suppliers

CYCLODECANOL 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: C1CCCCC(CCCC1)O

Technology Process of Cyclodecanol

There total 17 articles about Cyclodecanol 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: 95.0%

cyclodecane (293-96-9) → cyclodecanol (1502-05-2)

Guidance literature:

With ferredoxin reductase; [2Fe–2S] ferredoxin; cytochrome P₄₅₀ enzyme CYP₁₀₁B₁; In aq. buffer; pH=7.4; Reagent/catalyst; Kinetics; Catalytic behavior; Enzymatic reaction;

DOI:10.1039/d0cy01040e

Reference yield: 65.0%

cyclodecanone (1502-06-3) → cyclodecanol (1502-05-2)

Guidance literature:

With methanol; at 20 ℃; for 12h; UV-irradiation;

DOI:10.1016/S0040-4039(99)01357-X

Reference yield:

4-Nitro-benzenecarboperoxoic acid 1-cyclodecyl-1-methyl-ethyl ester → cyclodecanol (1502-05-2) + acetone (67-64-1) + 4-nitro-benzoic acid (62-23-7)

Guidance literature:

In methanol; at 25 ℃; Rate constant; Mechanism;

DOI:10.1016/S0040-4039(01)81913-4

upstream raw materials:

cyclodecanone

1,2-cyclodecadiene

trans-5,6-epoxy-cis-cyclodecene

toluene-4-sulfonic acid cyclodecyl ester

Downstream raw materials:

(Z)-cyclodecene

cyclodecanone

9-phenyl-9H-xanthene

cis-1,2-epoxy-cyclodecane

Refernces

• 1、 Zemlyakov,Tsikalova,Tsikalov. "Synthesis of β-cycloalkylglycosides of Muramyl Dipeptide". . p. 929 - 932. Retrieved 2017.
• 2、 Devaprabhakara,D.,Gardner,P.D.. "-". . p. 1458 - 1460. Retrieved 1963.
• 3、 Ito, Satoru,Ziffer, Herman,Box, Ad. "On the Relation between Ring Size and Geometry of 2-Bromo-2-cycloalkenyl Acetates Formed from Dibromobicycloalkanes by Silver Acetate Catalyzed Reactions. Use of 3J(C-H) Couplings To Assign the Geometry of Trisubstituted Olefins". . p. 1130 - 1133. Retrieved 1986.
• 4、 Sarkar, Md Raihan,Dasgupta, Samrat,Pyke, Simon M.,Bell, Stephen G.. "Selective biocatalytic hydroxylation of unactivated methylene C-H bonds in cyclic alkyl substrates". supporting information. p. 5029 - 5032. Retrieved 2019/05/21.