112279-72-8 | 4-Bromo-2,3-difluoroaniline

Packsize	Purity	Availability	Price	Discounted Price
100mg	97%	in stock	$8.00	$5.00
250mg	97%	in stock	$9.00	$6.00
1g	97%	in stock	$16.00	$12.00
5g	97%	in stock	$35.00	$25.00
10g	97%	in stock	$69.00	$49.00

Description

• Catalog Number: AD41656
• Chemical Name: 4-Bromo-2,3-difluoroaniline
• CAS Number: 112279-72-8
• Molecular Formula: C6H4BrF2N
• Molecular Weight: 208.0035
• MDL Number: MFCD09030643
• SMILES: Nc1ccc(c(c1F)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

4-Bromo-2,3-difluoroaniline is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the development of various pharmaceuticals, agrochemicals, and materials.One key application of 4-Bromo-2,3-difluoroaniline in chemical synthesis is its role as a precursor for the synthesis of diverse biologically active molecules. Its functional groups allow for selective modification at different positions, enabling the synthesis of complex structures with specific properties. This compound is often utilized in the pharmaceutical industry to create novel drug candidates with enhanced biological activity or improved pharmacokinetic profiles.Furthermore, 4-Bromo-2,3-difluoroaniline can participate in various coupling reactions, including Suzuki, Heck, and Buchwald-Hartwig couplings, facilitating the formation of carbon-carbon and carbon-heteroatom bonds. These synthetic transformations are crucial for the construction of complex organic molecules and natural product synthesis.Additionally, this compound can undergo various functional group transformations such as halogenation, arylation, and nucleophilic substitution, expanding its utility in organic synthesis. Its unique combination of bromo and difluoro substituents imparts specific electronic and steric effects, influencing the reactivity and selectivity of chemical reactions.Overall, 4-Bromo-2,3-difluoroaniline plays a vital role in the field of chemical synthesis, enabling the creation of diverse compounds with potential applications in medicine, agriculture, and materials science.