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AA55870

122455-37-2 | 3-Fluoro-2-iodoaniline hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $19.00 $13.00 -   +
250mg 97% in stock $23.00 $16.00 -   +
1g 97% in stock $40.00 $28.00 -   +
5g 97% in stock $178.00 $124.00 -   +
10g 97% in stock $306.00 $214.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA55870
Chemical Name: 3-Fluoro-2-iodoaniline hydrochloride
CAS Number: 122455-37-2
Molecular Formula: C6H6ClFIN
Molecular Weight: 273.4744132
MDL Number: MFCD19982814
SMILES: Ic1c(N)cccc1F.Cl

 

Computed Properties
Complexity: 99.1  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  

 

 

Upstream Synthesis Route
  • 3-Fluoro-2-iodoaniline hydrochloride is a versatile compound that finds extensive use in modern chemical synthesis processes. As a key building block in organic chemistry, this compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure allows for strategic incorporation of fluorine and iodine functionalities in target molecules, offering a valuable tool for medicinal chemists and process chemists alike. In drug discovery and development, 3-Fluoro-2-iodoaniline hydrochloride can serve as a valuable intermediate in the synthesis of bioactive compounds, facilitating the exploration of structure-activity relationships and enabling the modification of key pharmacophores. This compound also holds significance in the field of materials science, where its controlled introduction into polymer chains can impart desirable properties such as enhanced thermal stability and improved adhesion. Additionally, its selective reactivity in cross-coupling reactions makes it a sought-after reagent for the construction of complex molecular architectures. Overall, the application of 3-Fluoro-2-iodoaniline hydrochloride in chemical synthesis underscores its importance as a powerful tool for the development of novel compounds with diverse functionalities and applications.
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