5763-55-3

Basic information

• Product Name: 2-CYCLOPENTYL-ETHYLAMINE
• Synonyms: RARECHEM AN KA 1223;AKOS BC-0008;2-CYCLOPENTYL-ETHYLAMINE;CHEMBRDG-BB 4015075;(2-cyclopentylethyl)amine hydrochloride;(2-cyclopentylethyl)amine(SALTDATA: HCl);2-cyclopentylethan-1-aMine;CyclopentaneethanaMine
• CAS NO: 5763-55-3
• Molecular Formula: C₇H₁₅N
• Molecular Weight: 113.2
• Mol File: 5763-55-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 144.4 °C at 760 mmHg
• Flash Point: 35.4 °C
• Appearance: /
• Density: 0.871 g/cm³
• Vapor Pressure: 5.09mmHg at 25°C
• Refractive Index: 1.464
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 10.72±0.10(Predicted)
• CAS DataBase Reference: 2-CYCLOPENTYL-ETHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-CYCLOPENTYL-ETHYLAMINE(5763-55-3)
• EPA Substance Registry System: 2-CYCLOPENTYL-ETHYLAMINE(5763-55-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• HazardClass: IRRITANT
• Hazardous Substances Data: 5763-55-3(Hazardous Substances Data)

Usage

General Description

2-CYCLOPENTYL-ETHYLAMINE is a chemical compound that belongs to the class of organic compounds known as amines. It is a tertiary amine with a cyclopentyl substituent attached to the nitrogen atom. 2-CYCLOPENTYL-ETHYLAMINE is used in various industrial applications, including as a building block in the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential use in organic synthesis and as a reagent in chemical reactions. Additionally, 2-CYCLOPENTYL-ETHYLAMINE has been investigated for its potential role in the treatment of neurological disorders and for its use as a chiral auxiliary in asymmetric synthesis.

InChI:InChI=1/C7H15N/c8-6-5-7-3-1-2-4-7/h7H,1-6,8H2

Upstream product

• 5732-87-6 2-cyclopentylacetonitrile 
• 13988-39-1 chloromethylcyclopentane 
• 933-04-0 2-cyclopentylacetamide 
• 1123-00-8 2-cyclopentylacetic acid 
• 1122-99-2 2-cyclopentylacetyl chloride 
• 3197-72-6 2-(cyclopent-1-en-1-yl) ethan-1-amine 

Downstream Products

• 861081-64-3 N-(2-cyclopentyl-ethyl)-benzamide 
• 24321-79-7 2-(Cyclopentyl)-ethyl-isothiocyanat 
• 676495-35-5 6-[4-((2-cyclopentyl-ethyamino)-methyl)-2-ethoxyphenoxy]nicotinonitrile 
• 1072649-91-2 C₂₆H₃₄FN₃O₃ 
• 925898-42-6 N₃-(6-aminopyridin-3-yl)-N₁-(2-cyclopentylethyl)-4-methylisophthalamide 

Relevant articles and documents

Photoinduced remote regioselective radical alkynylation of unactivated C-H bonds

A method for the remote regioselective alkynylation of unactivated C(sp3)-H bonds in diverse aliphatic amides by photogenerated amidyl radicals has been developed. The site-selectivity is dominated via a 1,5-hydrogen atom transfer (HAT) process of the amide. Mild reaction conditions and high regioselectivity are demonstrated in this methodology.

Efficient preparation and application of monodisperse palladium loaded graphene oxide as a reusable and effective heterogeneous catalyst for suzuki cross-coupling reaction

A homogeneously dispersed graphene oxide supported palladium nanomaterial (Pd?GO) has been successfully synthesized and used as a catalyst in cross-coupling reactions at room temperature. Various analytical techniques such as X-ray Diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HR-TEM) were used to characterize the monodisperse Pd?GO. Monodisperse Pd?GO nanomaterials were used for the cross-coupling reactions which brought together organic molecules with functional significance. This catalyst showed superior catalytic activity and stability for these coupling reactions. High product yields, short reaction times and mild reaction conditions, obtained by the using of developed catalysts. Importantly, the catalyst can be used at least five experiments successfully without losing its efficiency.

Copper-Catalyzed Amide Radical-Directed Cyanation of Unactivated Csp3-H Bonds

A method for site-selective intermolecular δ/?-Csp3-H cyanation of aliphatic sulfonamides is developed using TsCN as the cyanating reagent, catalyzed by a Cu(I)/phenanthroline complex. The mild, expeditious, and modular protocol allows efficient remote Csp3-H cyanation with good functional group tolerance and high regioselectivity. Mechanistic studies indicate that the reaction might proceed through a Cu(I)-mediated N-F bond cleavage to generate an amidyl radical, 1,5-HAT, and cyano group transfer of the resulting carbon radical with TsCN.