16372-96-6 | 3,5-Dibromo-1-phenyl benzene

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$50.00	$35.00
5g	97%	in stock	$122.00	$86.00
10g	97%	in stock	$203.00	$142.00
25g	99%	in stock	$365.00	$255.00
100g	97%	in stock	$1,039.00	$728.00

Description

• Catalog Number: AA85801
• Chemical Name: 3,5-Dibromo-1-phenyl benzene
• CAS Number: 16372-96-6
• Molecular Formula: C12H8Br2
• Molecular Weight: 311.9999
• MDL Number: MFCD00143073
• SMILES: Brc1cc(Br)cc(c1)c1ccccc1

Computed Properties

• Complexity: 165
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Rotatable Bond Count: 1
• XLogP3: 4.9

Upstream Synthesis Route

3,5-Dibromo-1,1''-biphenyl is a versatile compound widely used in chemical synthesis for its unique reactivity and structural properties. In organic chemistry, this specific derivative of biphenyl serves as a valuable building block for the synthesis of various organic compounds. One of the key applications of 3,5-Dibromo-1,1''-biphenyl is in the preparation of biaryl compounds. By utilizing its bromine atoms as reactive sites, chemists can employ Suzuki-Miyaura coupling reactions to form carbon-carbon bonds between different aryl groups. This reaction is crucial in the construction of complex molecular structures found in pharmaceuticals, agrochemicals, and materials science.Furthermore, 3,5-Dibromo-1,1''-biphenyl can also participate in other cross-coupling reactions such as Heck coupling and Sonogashira coupling, enabling the synthesis of diverse organic molecules with specific functions and properties.Overall, the strategic placement of bromine atoms in 3,5-Dibromo-1,1''-biphenyl makes it a valuable tool in modern organic synthesis, facilitating the creation of structurally intricate and biologically active compounds.