3-Pentanamine, 3-ethyl-, hydrochloride

Base Information

• Chemical Name: 3-Pentanamine, 3-ethyl-, hydrochloride
• CAS No.: 56065-46-4
• Molecular Formula: C7H18ClN
• Molecular Weight: 151.6775
• European Community (EC) Number: 838-417-2
• DSSTox Substance ID: DTXSID10204613
• Mol file: 56065-46-4.mol

Synonyms:56065-46-4;3-ethylpentan-3-amine hydrochloride;3-Pentanamine, 3-ethyl-, hydrochloride;LCG 21558;(1,1-Diethylpropyl)amine hydrochloride;3-Ethyl-3-pentanamine hydrochloride;3-ethylpentan-3-amine;hydrochloride;SCHEMBL17363194;DTXSID10204613;3-ethylpentan-3-aminehydrochloride;MFCD01709390;AKOS026741123;BS-39553;LS-101534;EN300-85539

Chemical Property of 3-Pentanamine, 3-ethyl-, hydrochloride

Chemical Property:

• Vapor Pressure: 7.86mmHg at 25°C
• Boiling Point: 135.1°C at 760 mmHg
• Flash Point: 29.6°C
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 151.1127773
• Heavy Atom Count: 9
• Complexity: 47.1

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC(CC)(CC)N.Cl

Technology Process of 3-Pentanamine, 3-ethyl-, hydrochloride

There total 1 articles about 3-Pentanamine, 3-ethyl-, hydrochloride 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:

3-ethylpentane (617-78-7) → 3-ethylpentan-1-amine hydrochloride (1210414-12-2) + 3-ethylpentan-2-amine hydrochloride + 3-Ethylpentane-3-amine hydrochloride (56065-46-4)

Guidance literature:

3-ethylpentane; With cerium(III) chloride; 1,1,1-trichloroethanol; di-tert-butyl-diazodicarboxylate; tetrabutyl-ammonium chloride; In acetonitrile; at 20 ℃; for 18h; Irradiation; Inert atmosphere; Sealed tube;

With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 1h; Reagent/catalyst; Further stages;

DOI:10.1021/jacs.0c00212

upstream raw materials:

3-ethylpentane

Refernces