cyclopentyl acetate

Base Information

• Chemical Name: cyclopentyl acetate
• CAS No.: 933-05-1
• Molecular Formula: C7H12 O2
• Molecular Weight: 128.171
• Hs Code.: 2915390090
• European Community (EC) Number: 213-264-9
• NSC Number: 55885
• DSSTox Substance ID: DTXSID20239370
• Nikkaji Number: J100.652E
• Wikidata: Q83121719
• Mol file: 933-05-1.mol

Synonyms:Cyclopentanol,acetate (6CI,7CI,8CI,9CI); Cycloamyl acetate; Cyclopentyl acetate; NSC 55885

Chemical Property of cyclopentyl acetate

Chemical Property:

• Vapor Pressure: 2.55mmHg at 25°C
• Refractive Index: 1.4530 (estimate)
• Boiling Point: 159°Cat760mmHg
• Flash Point: 43.6°C
• PSA: 26.30000
• Density: 0.98g/cm³
• LogP: 1.49210
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 128.083729621
• Heavy Atom Count: 9
• Complexity: 104

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)OC1CCCC1

Technology Process of cyclopentyl acetate

There total 28 articles about cyclopentyl acetate 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: 97.0%

Cyclopentanol (96-41-3) + acetic anhydride (108-24-7) → cyclopentyl acetate (933-05-1)

Guidance literature:

With tris(pentafluorophenyl)borate; In neat (no solvent); at 20 ℃; for 0.0333333h; Green chemistry;

DOI:10.1016/j.tetlet.2014.01.124

Reference yield: 97.0%

Cyclopentanol (96-41-3) + ethyl acetate (141-78-6) → cyclopentyl acetate (933-05-1)

Guidance literature:

With 1,3-dicyclohexylimidazol-2-ylidene; at 25 ℃; for 0.5h;

DOI:10.1021/jo035431p

Reference yield: 97.0%

vinyl acetate (108-05-4,9003-20-7) + cyclopentene (142-29-0) → cyclopentyl acetate (933-05-1)

Guidance literature:

With ruthenium hydroxide trichloride; In dichloromethane; at 180 ℃; for 3h; Autoclave; Inert atmosphere;

DOI:10.1134/S1070428011020011

upstream raw materials:

Cyclopentyl bromide

silver(I) acetate

Perbenzoic acid

chloroform

Downstream raw materials:

1-(cyclopent-1-en-1-yl)ethanone

1,5-pentanedioic acid

N-cyclopentyl-4-methoxybenzamide

N-cyclopentylbenzamide

Refernces

• 1、 Khaligh, Nader Ghaffari,Mihankhah, Taraneh,Johan, Mohd Rafie,Juan, Joon Ching. "4-Imidazol-1-yl-butane-1-sulfonic acid ionic liquid: Synthesis, structural analysis, physical properties and catalytic application as dual solvent-catalyst". . p. 866 - 878. Retrieved 2019/07/12.
• 2、 Zheng, Guocai,Li, Xinzhong. "Consecutive addition esterification and hydrolysis of cyclic olefins catalyzed by multi-SO3H functionalized multi heteropolyanion-based ionic hybrids undersolvent-free conditions". . p. 933 - 941. Retrieved 2019/03/17.