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Cyclohexane, (diethoxymethyl)-

Base Information
  • Chemical Name:Cyclohexane, (diethoxymethyl)-
  • CAS No.:14315-64-1
  • Molecular Formula:C11H22O2
  • Molecular Weight:186.294
  • Hs Code.:
  • DSSTox Substance ID:DTXSID90449207
  • Nikkaji Number:J1.992.073I
  • Wikidata:Q82268603
  • Mol file:14315-64-1.mol
Cyclohexane, (diethoxymethyl)-

Synonyms:Cyclohexane, (diethoxymethyl)-;14315-64-1;Cyclohexanecarbaldehyde diethyl acetal;cyclohexanealdehyde diethylacetal;SCHEMBL14743720;DTXSID90449207

Suppliers and Price of Cyclohexane, (diethoxymethyl)-
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The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of Cyclohexane, (diethoxymethyl)-
Chemical Property:
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:5
  • Exact Mass:186.161979940
  • Heavy Atom Count:13
  • Complexity:113
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOC(C1CCCCC1)OCC
Technology Process of Cyclohexane, (diethoxymethyl)-

There total 7 articles about Cyclohexane, (diethoxymethyl)- 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 Pd(PhCN)2(OTf)2; at 20 ℃; for 0.25h; Inert atmosphere;
DOI:10.1055/s-0039-1690497
Guidance literature:
With C3H6NO9P3(6-)*4H2O*Cl(1-)*Gd(3+)*4H(1+); at 35 ℃; for 1h; Inert atmosphere;
DOI:10.1002/chem.201602157
Guidance literature:
With 1-diphenylphosphino-8-triphenylstibonium-naphthalene triflate; In neat liquid; at 20 ℃; for 0.16h; Inert atmosphere; Schlenk technique; Green chemistry;
DOI:10.1039/c6gc03629e
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