74553-29-0 | 2,5-Dibromobenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$11.00	$8.00
5g	98%	in stock	$19.00	$14.00
10g	98%	in stock	$23.00	$17.00
25g	98%	in stock	$56.00	$40.00
100g	98%	in stock	$203.00	$143.00

Description

• Catalog Number: AB60388
• Chemical Name: 2,5-Dibromobenzaldehyde
• CAS Number: 74553-29-0
• Molecular Formula: C7H4Br2O
• Molecular Weight: 263.9141
• MDL Number: MFCD00462864
• SMILES: O=Cc1cc(Br)ccc1Br

Computed Properties

• Complexity: 127
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.8

Upstream Synthesis Route

2,5-Dibromobenzaldehyde is a versatile compound that finds wide application in chemical synthesis, particularly in organic chemistry. This compound serves as a key building block for the synthesis of various important organic molecules due to its unique reactivity and structural properties. One prominent use of 2,5-Dibromobenzaldehyde is as a precursor in the synthesis of pharmaceutical compounds and agrochemicals. Its presence in the molecular structure of these bioactive molecules imparts desirable properties that are crucial for their biological activity. Additionally, 2,5-Dibromobenzaldehyde is employed in the preparation of dyes, polymers, and other specialty chemicals, showcasing its significance in the realm of industrial chemistry. Its ability to undergo a diverse range of chemical transformations makes it a valuable tool for organic chemists seeking to access complex molecular architectures efficiently. Furthermore, the unique reactivity of 2,5-Dibromobenzaldehyde enables the selective introduction of functional groups at specific positions in the molecule, allowing for precise control over the synthetic pathway. In summary, the application of 2,5-Dibromobenzaldehyde in chemical synthesis plays a crucial role in enabling the efficient and controlled construction of a wide variety of organic molecules with diverse applications.

Literature

• Synthesis and optical properties of isomeric branched pi-conjugated systems.

  The Journal of organic chemistry 20050916