2-Ethoxypentane

Base Information

• Chemical Name: 2-Ethoxypentane
• CAS No.: 1817-89-6
• Molecular Formula: C7H16 O
• Molecular Weight: 116.203
• Hs Code.: 2909199090
• DSSTox Substance ID: DTXSID40883753
• Nikkaji Number: J421.593A
• Mol file: 1817-89-6.mol

Synonyms:2-Ethoxypentane;1817-89-6;Pentane, 2-ethoxy-;Ethyl 1-methylbutyl ether;sec-Amyl ethyl ether;Propylather;SCHEMBL3315438;DTXSID40883753;MFCD00043661;AKOS006272613;FT-0612217

Chemical Property of 2-Ethoxypentane

Chemical Property:

• Vapor Pressure: 29.6mmHg at 25°C
• Melting Point: -95.35°C (estimate)
• Refractive Index: 1.3897 (estimate)
• Boiling Point: 109°Cat760mmHg
• Flash Point: 9°C
• PSA: 9.23000
• Density: 0.77g/cm³
• LogP: 2.21150
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 116.120115130
• Heavy Atom Count: 8
• Complexity: 43.7

Purity/Quality:

98%Min ^*data from raw suppliers

2-Ethoxypentane ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCC(C)OCC

Technology Process of 2-Ethoxypentane

There total 5 articles about 2-Ethoxypentane 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: 35.0%

ethanol (64-17-5) + 2-pentylamine (625-30-9) → 1-methylbutyl ethyl ether (1817-89-6)

Guidance literature:

With 7-phenyl-5,6,8,9-tetrahydrodibenzoxanthylium trifluoromethanesulphonate; triethylamine; at 25 ℃; for 96h;

Reference yield:

ethanol (64-17-5) + 1-penten (109-67-1) → 1-ethoxypentane (17952-11-3) + 1-methylbutyl ethyl ether (1817-89-6)

Guidance literature:

With heptamethyl methylaquacobyrinate perchlorate; oxygen; at 20 ℃; for 150h; Mechanism; Product distribution; Irradiation; other catalyst;

DOI:10.1246/bcsj.58.2652

Reference yield:

(S)-2-pentanol (26184-62-3) + ethyl iodide (75-03-6) → 1-methylbutyl ethyl ether (1817-89-6)

Guidance literature:

upstream raw materials:

(S)-2-pentanol

ethyl iodide

ethanol

1-penten

Refernces

• 1、 Murakami,Hisaeda. "Hydrophobic vitamin B12. IV. Addition reactions of alcohols to olefins as catalyzed by hydrophobic vitamin B12 derivatives". . p. 2652 - 2658. Retrieved 2007/10/02.