2-Pentyl-1,3-dioxolane

Base Information

• Chemical Name: 2-Pentyl-1,3-dioxolane
• CAS No.: 3515-94-4
• Molecular Formula: C8H16 O2
• Molecular Weight: 144.214
• Hs Code.: 2932999099
• European Community (EC) Number: 222-519-3
• DSSTox Substance ID: DTXSID20188652
• Nikkaji Number: J216.165F
• Wikidata: Q83060470
• Mol file: 3515-94-4.mol

Synonyms:2-Pentyl-1,3-dioxolane;3515-94-4;EINECS 222-519-3;2-n-pentyl-1,3 dioxolane;2-pentyl-[1,3]dioxolane;SCHEMBL4792651;DTXSID20188652;AKOS006278251

Chemical Property of 2-Pentyl-1,3-dioxolane

Chemical Property:

• Vapor Pressure: 1.67mmHg at 25°C
• Boiling Point: 173.7°Cat760mmHg
• Flash Point: 56.9°C
• PSA: 18.46000
• Density: 0.913g/cm³
• LogP: 1.93960
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 144.115029749
• Heavy Atom Count: 10
• Complexity: 77.3

Purity/Quality:

98%Min ^*data from raw suppliers

2-PENTYL-1,3-DIOXOLANE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCC1OCCO1

Technology Process of 2-Pentyl-1,3-dioxolane

There total 10 articles about 2-Pentyl-1,3-dioxolane 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: 100.0%

ethylene glycol (107-21-1) + hexanal (66-25-1) → 2-pentyl-1,3-dioxolane (3515-94-4)

Guidance literature:

distannoxane 1a; In benzene; for 0.5h; Mechanism; Product distribution; Heating; other distannoxane catalysts, other aldehydes, other alcohol, other solvents, other reaction times;

DOI:10.1016/S0040-4020(01)92233-1

Reference yield: 100.0%

ethylene glycol (107-21-1) → 2-pentyl-1,3-dioxolane (3515-94-4)

Guidance literature:

distannoxane 1a; In benzene; for 0.5h; Heating;

DOI:10.1016/S0040-4020(01)92233-1

Reference yield: 92.0%

2-(5-chloropentyl)-1,3-dioxolane (114905-18-9) → 2-pentyl-1,3-dioxolane (3515-94-4)

Guidance literature:

With naphthalene; lithium; In tetrahydrofuran; at -78 ℃; for 2.5h;

upstream raw materials:

ethylene glycol

hexanal

2-(5-chloropentyl)-1,3-dioxolane

ethene

Downstream raw materials:

methyl hexanoate

2-(1-Chloro-pentyl)-[1,3]dioxolane

2-bromoethyl hexanoate

2-undecanyl-1,3-dioxolane

Refernces

• 1、 Zhao, Shen,Jia, Yueqing,Song, Yu-Fei. "Acetalization of aldehydes and ketones over H4[SiW 12O40] and H4[SiW12O 40]/SiO2". . p. 2618 - 2625. Retrieved 2014/07/22.
• 2、 Aliyan, Hamid,Fazaeli, Razieh,Massah, Ahmad Reza,Momeni, Ahmad Reza,Naghash, Hamid Javaherian,Moeinifard, Behzad. "Acetalization of carbonyl compounds catalyzed by bismuth triflate under solvent-free conditions". experimental part. p. 873 - 876. Retrieved 2012/04/05.