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AB87458

89510-90-7 | 2-Chloro-5-fluoropyridin-4-amine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $8.00 $6.00 -   +
1g 98% in stock $19.00 $14.00 -   +
5g 98% in stock $85.00 $60.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB87458
Chemical Name: 2-Chloro-5-fluoropyridin-4-amine
CAS Number: 89510-90-7
Molecular Formula: C5H4ClFN2
Molecular Weight: 146.5501
MDL Number: MFCD16622225
SMILES: Clc1ncc(c(c1)N)F

 

Computed Properties
Complexity: 101  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.2  

 

 

Upstream Synthesis Route
  • 2-Chloro-5-fluoro-4-pyridinamine, also known as $name$, is a key reagent widely used in chemical synthesis. This compound plays a crucial role in organic chemistry reactions due to its unique properties and versatility.Its application in chemical synthesis is particularly notable in the pharmaceutical industry, where it serves as a building block for the production of various drug compounds. $Name$ is commonly employed in the synthesis of pharmaceutical intermediates and active ingredients due to its ability to participate in a wide range of reactions.One of the primary functions of 2-Chloro-5-fluoro-4-pyridinamine in chemical synthesis is as a nucleophilic reagent. It can act as a nucleophile in substitution reactions, where it replaces a leaving group on a molecule, leading to the formation of new bonds and the creation of more complex structures. This reactivity makes $name$ a valuable tool for the construction of diverse chemical compounds.Additionally, $name$ can also participate in various coupling reactions, serving as a coupling partner to form carbon-carbon or carbon-heteroatom bonds. This capability further expands its utility in chemical synthesis by enabling the creation of intricate molecular architectures.Overall, the unique properties and reactivity of 2-Chloro-5-fluoro-4-pyridinamine make it an indispensable component in the toolkit of synthetic chemists, particularly in the pharmaceutical and related industries. Its versatile applications and ability to facilitate a wide range of reactions highlight its importance in advancing the field of organic chemistry and drug discovery.
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