AB87458
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.
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 |
Complexity: | 101 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
XLogP3: | 1.2 |
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.