156682-52-9 | 1,4-Dibromo-2,3-difluorobenzene

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$11.00	$8.00
5g	97%	in stock	$21.00	$15.00
10g	97%	in stock	$31.00	$22.00
25g	97%	in stock	$60.00	$42.00
50g	97%	in stock	$100.00	$70.00
100g	97%	in stock	$195.00	$137.00
500g	97%	in stock	$974.00	$682.00

Description

• Catalog Number: AA78734
• Chemical Name: 1,4-Dibromo-2,3-difluorobenzene
• CAS Number: 156682-52-9
• Molecular Formula: C6H2Br2F2
• Molecular Weight: 271.8849
• MDL Number: MFCD09835192
• SMILES: Fc1c(Br)ccc(c1F)Br

Computed Properties

• Complexity: 106
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• XLogP3: 3.5

Upstream Synthesis Route

1,4-Dibromo-2,3-difluorobenzene is a versatile compound that finds extensive applications in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a valuable building block in the creation of various complex organic molecules and pharmaceuticals. Due to its unique structure and reactivity, 1,4-Dibromo-2,3-difluorobenzene is utilized in the synthesis of specialty chemicals, agrochemicals, and materials science.One of the key applications of 1,4-Dibromo-2,3-difluorobenzene is in cross-coupling reactions, where it acts as an effective precursor for the introduction of functional groups into organic molecules. This compound can undergo various reactions such as Suzuki cross-coupling, Stille coupling, and Heck reaction, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Additionally, 1,4-Dibromo-2,3-difluorobenzene is employed in the synthesis of biologically active compounds and fluorescent materials, showcasing its significance in drug discovery and materials science research.Moreover, the presence of bromine and fluorine atoms in the molecular structure of 1,4-Dibromo-2,3-difluorobenzene imparts desirable properties to the derived products, making it a valuable starting material for the development of advanced materials with specific properties. Its ability to undergo diverse chemical transformations makes it a vital component in the toolbox of synthetic chemists looking to access novel molecules for various applications.