122375-82-0 | 2-Bromo-4,5,6-trifluoroaniline

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$19.00	$13.00
5g	95%	in stock	$40.00	$28.00
10g	95%	in stock	$65.00	$45.00
25g	95%	in stock	$103.00	$72.00

Description

• Catalog Number: AB61350
• Chemical Name: 2-Bromo-4,5,6-trifluoroaniline
• CAS Number: 122375-82-0
• Molecular Formula: C6H3BrF3N
• Molecular Weight: 225.9939
• MDL Number: MFCD12756457
• SMILES: Brc1cc(F)c(c(c1N)F)F

Computed Properties

• Complexity: 146
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• XLogP3: 2.2

Upstream Synthesis Route

6-Bromo-2,3,4-trifluoroaniline is a versatile chemical compound widely used in chemical synthesis processes as a key building block. Its unique structure containing bromine and trifluoromethyl groups makes it a valuable intermediate for the synthesis of various functional molecules. One of the key applications of 6-Bromo-2,3,4-trifluoroaniline is its role as a valuable starting material in the pharmaceutical industry. It serves as a crucial intermediate in the synthesis of pharmaceutical compounds, particularly those with fluorinated aromatic structures. The bromine and trifluoromethyl groups present in this compound can be selectively substituted or functionalized to introduce specific pharmacological properties required for drug development.In addition to its pharmaceutical applications, 6-Bromo-2,3,4-trifluoroaniline is also utilized in the preparation of agrochemicals and advanced materials. Its versatile reactivity allows for the modification of its chemical structure to tailor properties such as solubility, stability, and activity, making it a valuable component in the design of specialized chemicals for various industrial applications.Furthermore, 6-Bromo-2,3,4-trifluoroaniline plays a significant role in academic research and chemical synthesis, where its unique structural features can be harnessed for the design and creation of novel molecules with specific functions. Its presence in the synthetic chemist's toolbox enables the construction of complex molecular architectures through diverse chemical transformations, highlighting its importance in the field of organic chemistry.