1160573-67-0 | 1-Bromo-3-chloro-2,5-difluorobenzene

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$36.00	$25.00
250mg	98%	in stock	$48.00	$33.00
1g	98%	in stock	$58.00	$40.00
5g	98%	in stock	$165.00	$115.00
10g	98%	in stock	$299.00	$209.00
25g	98%	in stock	$573.00	$402.00
100g	98%	in stock	$1,536.00	$1,075.00

Description

• Catalog Number: AA14695
• Chemical Name: 1-Bromo-3-chloro-2,5-difluorobenzene
• CAS Number: 1160573-67-0
• Molecular Formula: C6H2BrClF2
• Molecular Weight: 227.43388639999998
• MDL Number: MFCD11845991
• SMILES: Fc1cc(Cl)c(c(c1)Br)F

Computed Properties

• Complexity: 122
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 3.4

Upstream Synthesis Route

1-Bromo-3-chloro-2,5-difluorobenzene, a versatile chemical compound, finds significant applications in organic synthesis as a key building block. With its unique structure and reactivity, this compound serves as a crucial intermediate in the production of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 1-Bromo-3-chloro-2,5-difluorobenzene acts as an important precursor in the formation of fluorinated aromatic compounds. Its halogen substituents enable selective functionalization reactions, allowing for the introduction of specific functional groups at precise positions on the benzene ring. This compound's reactivity and compatibility with a wide range of reaction conditions make it a valuable tool in the creation of complex molecules with tailored properties.Furthermore, 1-Bromo-3-chloro-2,5-difluorobenzene participates in cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds. These transformations enable the synthesis of diverse organic compounds, including pharmaceutical intermediates, agrochemicals, and materials for advanced applications. The presence of halogen atoms in the molecule enhances the reactivity and selectivity of these coupling reactions, making this compound a preferred choice in synthetic pathways requiring precise control over bond formation.Overall, the versatile nature of 1-Bromo-3-chloro-2,5-difluorobenzene makes it an indispensable tool in modern chemical synthesis, facilitating the construction of complex molecular structures with tailored functionalities and properties.