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AE42211

1262198-07-1 | 3-Bromo-2,6-difluoroaniline

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $6.00 $5.00 -   +
1g 98% in stock $19.00 $14.00 -   +
5g 98% in stock $85.00 $60.00 -   +
25g 98% in stock $386.00 $270.00 -   +
100g 98% in stock $1,317.00 $922.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE42211
Chemical Name: 3-Bromo-2,6-difluoroaniline
CAS Number: 1262198-07-1
Molecular Formula: C6H4BrF2N
Molecular Weight: 208.0035
MDL Number: MFCD22627833
SMILES: Fc1ccc(c(c1N)F)Br

 

Computed Properties
Complexity: 122  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
XLogP3: 2.1  

 

 

Upstream Synthesis Route
  • 3-Bromo-2,6-difluorobenzenamine, also known as $name$, serves a crucial role in chemical synthesis as a versatile building block. Its unique structure containing both bromine and fluorine atoms makes it highly valuable for the creation of various pharmaceuticals, agrochemicals, and materials.First and foremost, 3-Bromo-2,6-difluorobenzenamine is a key intermediate in the synthesis of complex molecules used in medicinal chemistry. Its ability to undergo various functional group transformations allows for the introduction of specific chemical moieties necessary for enhancing the biological activity of drug candidates. By strategically incorporating this compound into the molecular structure, researchers can modulate the pharmacokinetic and pharmacodynamic properties of the final product.Furthermore, this compound is utilized in the development of agrochemicals, including pesticides and herbicides. Its electron-withdrawing fluorine and bromine substituents can enhance the activity and selectivity of these crop protection agents, improving their effectiveness while minimizing environmental impact. Through targeted modifications of 3-Bromo-2,6-difluorobenzenamine, chemists can fine-tune the properties of agricultural chemicals to optimize their performance.In addition to its role in pharmaceuticals and agrochemicals, 3-Bromo-2,6-difluorobenzenamine finds application in materials science. By incorporating this compound into polymer chains or surface coatings, researchers can impart desired properties such as enhanced thermal stability, chemical resistance, or adhesion. The presence of the bromine and fluorine functionalities offers opportunities for introducing specific interactions or cross-linking mechanisms, leading to the development of advanced materials with tailored characteristics.Overall, 3-Bromo-2,6-difluorobenzenamine plays a crucial role in chemical synthesis by serving as a versatile and strategic building block for creating a wide range of valuable compounds in the fields of pharmaceuticals, agrochemicals, and materials science.
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