Cyclopentylisopropylamine hydrochloride

Base Information

• Chemical Name: Cyclopentylisopropylamine hydrochloride
• CAS No.: 52703-17-0
• Molecular Formula: C8H18ClN
• Molecular Weight: 163.68822
• Hs Code.: 2921300090
• European Community (EC) Number: 848-195-9
• DSSTox Substance ID: DTXSID10590462
• Mol file: 52703-17-0.mol

Synonyms:52703-17-0;Cyclopentylisopropylamine hydrochloride;1170802-25-1;N-(propan-2-yl)cyclopentanamine hydrochloride;N-cyclopentyl-N-isopropylamine hydrochloride;cyclopentyl-isopropyl-aminehydrochloride;cyclopentyl-isopropyl-amine hcl;Cyclopentyl-isopropyl-amine hydrochloride;N-propan-2-ylcyclopentanamine;hydrochloride;MFCD08689638;N-isopropylcyclopentanamine;N-ISOPROPYLCYCLOPENTANAMINE HYDROCHLORIDE;DTXSID10590462;Cyclopentyl-isopropyl-amine x HCl;CCA70317;AKOS015996612;DB-307781;CS-0245403;EN300-30451;G32720;Z316170330;N-(Propan-2-yl)cyclopentanamine--hydrogen chloride (1/1)

Chemical Property of Cyclopentylisopropylamine hydrochloride

Chemical Property:

• Vapor Pressure: 0.163mmHg at 25°C
• Refractive Index: ">
• Boiling Point: 210°Cat760mmHg
• PKA: 10.94±0.20(Predicted)
• Flash Point: 80.8°C
• PSA: 12.03000
• Density: g/cm³
• LogP: 3.11990
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 163.1127773
• Heavy Atom Count: 10
• Complexity: 72.6

Purity/Quality:

Cyclopentylisopropylaminehydrochloride 95+% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)NC1CCCC1.Cl

Technology Process of Cyclopentylisopropylamine hydrochloride

There total 3 articles about Cyclopentylisopropylamine 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: 10.0%

acetone (67-64-1) + Cyclopentamine (1003-03-8) → N-cyclopentylisopropylamine (52703-17-0)

Guidance literature:

With sodium tris(acetoxy)borohydride; acetic acid; In tetrahydrofuran; at 20 ℃; for 15h; Molecular sieve; Inert atmosphere;

DOI:10.1016/j.ejmech.2020.112961

Reference yield:

Cyclopentamine (1003-03-8) → N-cyclopentylisopropylamine (52703-17-0)

Guidance literature:

With Sodium triacetoxy borohydride; In acetone; at 20 ℃; for 24h;

Reference yield:

palladium dihydroxide + Cyclopentamine (1003-03-8) → N-cyclopentylisopropylamine (52703-17-0)

Guidance literature:

In acetone;

upstream raw materials:

Cyclopentamine

acetone

Downstream raw materials:

2,4-Dibromo-6-[(cyclopentyl-isopropyl-amino)-methyl]-phenol

N-cyclopentylbenzylamine

Refernces

• 1、 -. "Purine derivatives". Page column 35. . Retrieved 2010/02/04.
• 2、 -. "Purine derivatives". . . Retrieved 2008/06/13.