644985-24-0 | 4-Bromo-2,3-difluorobenzaldehyde

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$12.00	$9.00
5g	97%	in stock	$29.00	$20.00
10g	97%	in stock	$57.00	$40.00
25g	97%	in stock	$112.00	$79.00

Description

• Catalog Number: AB48759
• Chemical Name: 4-Bromo-2,3-difluorobenzaldehyde
• CAS Number: 644985-24-0
• Molecular Formula: C7H3BrF2O
• Molecular Weight: 220.9989264
• MDL Number: MFCD09258953
• SMILES: O=Cc1ccc(c(c1F)F)Br

Computed Properties

• Complexity: 153
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• XLogP3: 2.3

Upstream Synthesis Route

4-Bromo-2,3-difluorobenzaldehyde, a versatile chemical compound, plays a crucial role in chemical synthesis. This compound is commonly utilized as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. Its unique structure and reactivity make it a valuable intermediate in the synthesis of complex organic molecules.In chemical synthesis, 4-Bromo-2,3-difluorobenzaldehyde serves as a vital precursor for the preparation of diverse compounds due to its ability to participate in a wide range of reactions. Its bromine and difluoromethyl groups provide opportunities for selective functionalization, allowing chemists to introduce specific functional groups at precise positions on the benzene ring. This control over the chemical transformations enables the synthesis of structurally complex and bioactive molecules with high efficiency.Additionally, the presence of electron-withdrawing fluorine atoms enhances the reactivity and stability of 4-Bromo-2,3-difluorobenzaldehyde, making it a preferred reagent in cross-coupling reactions, aromatic substitutions, and other key synthetic processes. Its versatile nature and compatibility with various reaction conditions make it a valuable tool for chemists working in the fields of medicinal chemistry, materials science, and organic synthesis.In summary, the application of 4-Bromo-2,3-difluorobenzaldehyde in chemical synthesis showcases its significance as a pivotal building block for the construction of diverse organic compounds with specific functionalities and properties. Its versatility, reactivity, and structural features make it an indispensable reagent for the efficient and strategic synthesis of complex molecules in modern synthetic chemistry.