Cyclopentadecane

Base Information

• Chemical Name: Cyclopentadecane
• CAS No.: 295-48-7
• Molecular Formula: C15H30
• Molecular Weight: 210.403
• DSSTox Substance ID: DTXSID1059781
• Nikkaji Number: J79.584D
• Wikidata: Q17992517
• Mol file: 295-48-7.mol

Synonyms:Cyclopentadecane;295-48-7;EINECS 206-040-7;DTXSID1059781;MFCD00039424;AKOS025295076;AS-56765;C1224;CS-0320535;FT-0631905;D89373;1-(4-FLUOROPHENYL)PIPERAZINEHYDROCHLORIDE;Q17992517

Chemical Property of Cyclopentadecane

Chemical Property:

• Vapor Pressure: 0.00677mmHg at 25°C
• Melting Point: 64 °C
• Refractive Index: 1.45
• Boiling Point: 300.1 °C at 760 mmHg
• Flash Point: 124.9 °C
• PSA: 0.00000
• Density: 0.79 g/cm³
• LogP: 5.85150
• Solubility.: soluble in Acetone
• XLogP3: 8.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 0
• Exact Mass: 210.234750957
• Heavy Atom Count: 15
• Complexity: 58.6

Purity/Quality:

98%,99%, ^*data from raw suppliers

Cyclopentadecane >98.0%(GC) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn,Xi
• Hazard Codes: Xn,Xi

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCCCCCCCCCCCCC1

Technology Process of Cyclopentadecane

There total 22 articles about Cyclopentadecane 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: 80.0%

C15H16S2 → cyclopentadecane (295-48-7)

Guidance literature:

With Raney nickel; In ethanol; acetone; at 60 ℃; for 1h; Inert atmosphere;

DOI:10.1016/j.tetlet.2016.04.062

Reference yield: 71.0%

2-Nitrocyclopentadecanone (p-tolylsulfonyl)hydrazone (128780-81-4) → cyclopentadecane (295-48-7)

Guidance literature:

With lithium aluminium tetrahydride; In tetrahydrofuran; at 60 ℃; for 10h;

DOI:10.1021/jo00304a032

Reference yield: 22.0%

cyclohexanone triperoxide (182-01-4) → 15-hexadecanolide (109-29-5) + cyclopentadecane (295-48-7)

Guidance literature:

at 300 ℃; for 4h; Temperature; Flow reactor;

DOI:10.1021/acs.joc.1c00663

upstream raw materials:

cyclopentadecyne

cyclopentadecanone semicarbazone

sodium ethanolate

cyclopentadecanone

Downstream raw materials:

cyclopentadecanol

p-trifluoromethylphenyl bromide

C₁₆H₃₀F₃NO₂S

cyclopentadecanone

Refernces

• 1、 Trahanovsky, Walter S.,Klumpp, Douglas A.. "The chemistry of thiophene-based bis-(p-quinodimethanes): An approach to macrocycles". . p. 2386 - 2389. Retrieved 2016/05/19.
• 2、 Ahuja, Ritu,Kundu, Sabuj,Goldman, Alan S.,Brookhart, Maurice,Vicente, Brian C.,Scott, Susannah L.. "Catalytic ring expansion, contraction, and metathesis-polymerization of cycloalkanes". . p. 253 - 255. Retrieved 2008/03/13.