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2-aminocyclopentanemethylamine, with the molecular formula C6H13N, is a cyclic amine characterized by a pentagonal structure and a primary amine group. It serves as a versatile building block in organic synthesis and medicinal chemistry, playing a crucial role in the preparation of pharmaceuticals and bioactive molecules. Additionally, it exhibits potential as a ligand in coordination chemistry, further expanding its applications in the development of new drugs and the study of biological activities of various molecules.

21544-02-5

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21544-02-5 Usage

Uses

Used in Organic Synthesis:
2-aminocyclopentanemethylamine is used as a building block in organic synthesis for the preparation of various pharmaceuticals and bioactive molecules. Its unique cyclic structure and primary amine group enable the formation of diverse chemical compounds, contributing to the development of novel therapeutic agents.
Used in Medicinal Chemistry:
In medicinal chemistry, 2-aminocyclopentanemethylamine is utilized as a key component in the synthesis of pharmaceuticals. Its ability to form stable bonds with other molecules allows for the creation of new drug candidates with potential therapeutic benefits.
Used in Coordination Chemistry as a Ligand:
2-aminocyclopentanemethylamine also finds application in coordination chemistry, where it serves as a ligand. Its coordination with metal ions can lead to the formation of complexes with unique properties, which can be further explored for their potential applications in various fields, including catalysis and materials science.
Used in Drug Development:
The potential applications of 2-aminocyclopentanemethylamine extend to the development of new drugs. Its ability to interact with biological targets and modulate their activity makes it a promising candidate for the design of innovative therapeutic agents targeting various diseases and conditions.
Used in Biological Activity Studies:
Furthermore, 2-aminocyclopentanemethylamine is employed in the study of the biological activity of various molecules. Its incorporation into different chemical structures allows researchers to investigate its effects on biological systems, providing valuable insights into its potential therapeutic applications and mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 21544-02-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,4 and 4 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21544-02:
(7*2)+(6*1)+(5*5)+(4*4)+(3*4)+(2*0)+(1*2)=75
75 % 10 = 5
So 21544-02-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H14N2/c7-4-5-2-1-3-6(5)8/h5-6H,1-4,7-8H2

21544-02-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(aminomethyl)cyclopentan-1-amine

1.2 Other means of identification

Product number -
Other names 1-(Aminomethyl)-2-aminocyclopentane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:21544-02-5 SDS

21544-02-5Relevant academic research and scientific papers

Syntheses and biological activities of octahydro-1H-cyclopenta[d]pyrimidine derivatives

Tian, Zhongzhen,Jiang, Zhaoxing,Li, Zhong,Song, Gonghua,Huang, Qingchun

, p. 143 - 147 (2008/02/03)

Various nitromethylene derivatives were synthesized regioselectively. Compounds 8a-f were obtained by the reaction of 1-((5-chloropyridin-2-yl)methyl) -2-(nitromethylene)-octahydro-1H-cyclopenta[d]-pyrimidine (3) with primary amines and formaldehyde. The synthesized compounds were identified by 1H NMR, HRMS (EI), and IR, and preliminary bioassays indicated that most of them showed moderate insecticidal activities against Aphis craccivora. The relationship between hydrophobicity and biological activity was also discussed.

Low pressure process for the manufacture of 2-(aminomethyl)-1-cyclopentylamine

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Page 2, (2008/06/13)

Disclosed herein is a process for the manufacture of 2-(aminomethyl)-1-cyclopentylamine by low-pressure hydrogenation of 1-amino-2-cyano-1-cyclopentene using a combination catalyst system of nickel with palladium on carbon, or a single palladium-doped Raney-type catalyst.

Quinolones used as MRS inhibitors and bactericides

-

, (2008/06/13)

Compounds of formula (I) are inhibitors of the bacterial enzymeS aureusmethionyl tRNA synthetase and are of use in treating bacterial infections.

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