201138-91-2 | 4,6-Dibromodibenzofuran

Packsize	Purity	Availability	Price	Discounted Price
250mg	99%	in stock	$8.00	$5.00
1g	99%	in stock	$18.00	$12.00
5g	99%	in stock	$60.00	$42.00
10g	99%	in stock	$113.00	$79.00
25g	99%	in stock	$215.00	$150.00
100g	99%	in stock	$678.00	$474.00

Description

• Catalog Number: AB10230
• Chemical Name: 4,6-Dibromodibenzofuran
• CAS Number: 201138-91-2
• Molecular Formula: C12H6Br2O
• Molecular Weight: 325.9834
• MDL Number: MFCD00185686
• SMILES: Brc1cccc2c1oc1c2cccc1Br

Computed Properties

• Complexity: 222
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 1
• XLogP3: 5

Upstream Synthesis Route

4,6-Dibromodibenzo[b,d]furan, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. This compound is widely utilized in the preparation of various organic molecules due to its unique structural properties and reactivity. In organic synthesis, 4,6-Dibromodibenzo[b,d]furan serves as a key intermediate for the synthesis of biologically active compounds, pharmaceuticals, and advanced materials. Its bromine substituents provide anchoring points for further functionalization, allowing chemists to introduce a wide range of functional groups onto the dibenzofuran scaffold. This flexibility enables the creation of complex molecular structures with tailored properties and specific functionalities.Moreover, the presence of the dibenzofuran core in 4,6-Dibromodibenzo[b,d]furan confers aromaticity and stability to the molecule, making it a valuable precursor for the construction of aromatic compounds and heterocyclic systems. Through various synthetic transformations such as cross-coupling reactions, halogenation, and palladium-catalyzed coupling reactions, this compound can be transformed into diverse chemical entities with enhanced reactivity and biological activity.Overall, the strategic incorporation of 4,6-Dibromodibenzo[b,d]furan into chemical synthesis schemes offers chemists a powerful tool for designing and accessing novel molecular architectures with potential applications in drug discovery, material science, and organic electronics. Its versatility and adaptability make it an indispensable building block for the construction of complex organic molecules with tailored properties and functionalities.

Literature

• Formation of bromochlorodibenzo-p-dioxins and dibenzofurans from the high-temperature oxidation of a mixture of 2-chlorophenol and 2-bromophenol.

  Environmental science & technology 20060501

• Mechanisms of dioxin formation from the high-temperature oxidation of 2-bromophenol.

  Environmental science & technology 20050401

• Mechanisms of dioxin formation from the high-temperature pyrolysis of 2-bromophenol.

  Environmental science & technology 20031215