6053-58-3

Basic information

• Product Name: (3-CYCLOPENTYLPROPYL)AMINE
• Synonyms: (3-CYCLOPENTYLPROPYL)AMINE;(3-cyclopentylpropyl)amine(SALTDATA: FREE);CyclopentanepropanaMine;3-Cyclopentyl-1-propanamine
• CAS NO: 6053-58-3
• Molecular Formula: C₈H₁₇N
• Molecular Weight: 127.23
• Mol File: 6053-58-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 168.322°C at 760 mmHg
• Flash Point: 50.137°C
• Appearance: /
• Density: 0.869g/cm³
• Vapor Pressure: 1.628mmHg at 25°C
• Refractive Index: 1.466
• CAS DataBase Reference: (3-CYCLOPENTYLPROPYL)AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: (3-CYCLOPENTYLPROPYL)AMINE(6053-58-3)
• EPA Substance Registry System: (3-CYCLOPENTYLPROPYL)AMINE(6053-58-3)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36
• WGK Germany: 3
• Hazardous Substances Data: 6053-58-3(Hazardous Substances Data)

Usage

General Description

(3-CYCLOPENTYLPROPYL)AMINE is an organic compound that belongs to the class of amines. It is made up of a cyclopentyl ring attached to a propyl group, with an amine functional group at the end. This chemical is commonly used as a building block in organic synthesis and is employed in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals. It can also be utilized as an intermediate in the production of surfactants, ion exchange resins, and corrosion inhibitors. Additionally, (3-CYCLOPENTYLPROPYL)AMINE has applications in the synthesis of polymers and can be used as a catalyst in chemical reactions. Due to its versatile nature and the wide range of applications, this compound is of interest to researchers and the chemical industry.

InChI:InChI=1/C8H17N/c9-7-3-6-8-4-1-2-5-8/h8H,1-7,9H2

Upstream product

• 935-10-4 3-cyclopentylpropanamide 
• 104-97-2 cyclopentanepropanoyl chloride 
• 140-77-2 3-cyclopentylpropionic acid 
• 1123-04-2 3-cyclopentylpropionitrile 

Downstream Products

• 1355153-70-6 C₄₁H₄₀N₄O₂ 

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.

Cationic lipid compound, composition containing same and application

The invention provides a cationic lipid compound, a composition containing the cationic lipid compound and application of the cationic lipid compound. In order to provide more choices for delivery of preparations such as nucleic acid drugs, gene vaccines, small molecule drugs and the like, the invention provides a cationic lipid compound shown in the general formula or pharmaceutically available salts thereof. The cationic lipid compound provided by the invention can be used for delivering DNA, RNA or small molecule drugs, enriches the types of cationic lipid compounds, and has important significance for the development and application of nucleic acid preventive and therapeutic agents.

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.