6053-58-3

Usage

Uses

Used in Pharmaceutical Industry:
(3-CYCLOPENTYLPROPYL)AMINE is used as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents due to its unique structural properties and reactivity.
Used in Agrochemical Industry:
In the agrochemical sector, (3-CYCLOPENTYLPROPYL)AMINE is utilized as a precursor in the production of agrochemicals, playing a crucial role in the formulation of pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Specialty Chemicals Production:
(3-CYCLOPENTYLPROPYL)AMINE is employed as a building block in the synthesis of specialty chemicals, which are used in a wide range of applications, including coatings, adhesives, and sealants, due to its specific chemical characteristics.
Used in Surfactant Production:
(3-CYCLOPENTYLPROPYL)AMINE is used as an intermediate in the production of surfactants, which are essential in various industries for their properties to reduce surface tension and stabilize emulsions.
Used in Ion Exchange Resin Synthesis:
(3-CYCLOPENTYLPROPYL)AMINE is utilized in the synthesis of ion exchange resins, which are vital in water treatment and various industrial processes for their ability to remove ions from solutions.
Used in Corrosion Inhibitor Formulation:
As a component in the formulation of corrosion inhibitors, (3-CYCLOPENTYLPROPYL)AMINE helps protect materials from degradation in various industrial applications, extending the lifespan of equipment and structures.
Used in Polymer Synthesis:
(3-CYCLOPENTYLPROPYL)AMINE is used in the synthesis of polymers, contributing to the development of new materials with specific properties for use in plastics, textiles, and other industries.
Used as a Catalyst in Chemical Reactions:
(3-CYCLOPENTYLPROPYL)AMINE is also employed as a catalyst to facilitate various chemical reactions, enhancing the efficiency and selectivity of processes in the chemical industry.

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

Upstream product

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

Downstream Products

• 1355153-70-6 C₄₁H₄₀N₄O₂ 

Relevant academic research and scientific papers

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.

Remote Regioselective Radical C-H Functionalization of Unactivated C-H Bonds in Amides: The Synthesis of gem-Difluoroalkenes

The site-selective functionalization of unactivated aliphatic amines is an attractive and challenging synthetic approach. We herein report a general strategy for the remote site-selective functionalization of unactivated C(sp3)-H bonds in amides by photogenerated amidyl radicals to form gem-difluoroalkenes with trifluoromethyl-substituted alkenes. The site selectivity is controlled by a 1,5-hydrogen atom transfer (HAT) process of the amide. This photocatalyzed transformation shows both chemo- and site-selectivity, facilitating the formation of a secondary, tertiary, or quaternary carbon center.

Remote Directed Isocyanation of Unactivated C(sp3)-H Bonds: Forging Seven-Membered Cyclic Ureas Enabled by Copper Catalysis

Reported herein is an unprecedented copper-catalyzed site-selective ?-C(sp3)-H bonds activation of aliphatic sulfonamides for constructing the synthetically useful seven-membered N-heterocycles. A key to success is the use of in-situ-formed amide radicals, to activate the inert C(sp3)-H bond, and inexpensive TMSNCO, as a coupling reagent under mild conditions. To the best of our knowledge, this represents the first use of alkylamine derivatives as a five-membered synthon to prepare a seven-membered N-heterocycles.

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.

2,3,5-substituted biphenyls useful in the treatment of insulin resistance and hyperglycemia

This invention provides compounds of Formula I having the structure wherein:B, C, D, and R1 are as defined hereinbefore in the specification, or a pharmaceutically acceptable salt thereof, which are useful in treating metabolic disorders related to insulin resistance or hyperglycemia.