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AA47704

1326714-93-5 | 3-Bromo-2,4-difluorobenzaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $26.00 $18.00 -   +
250mg 95% in stock $39.00 $27.00 -   +
1g 95% in stock $45.00 $32.00 -   +
5g 95% in stock $142.00 $99.00 -   +
10g 95% in stock $219.00 $153.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA47704
Chemical Name: 3-Bromo-2,4-difluorobenzaldehyde
CAS Number: 1326714-93-5
Molecular Formula: C7H3BrF2O
Molecular Weight: 220.9989
MDL Number: MFCD22543686
SMILES: O=Cc1ccc(c(c1F)Br)F

 

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
  • 3-Bromo-2,4-difluorobenzaldehyde is a versatile chemical compound that finds wide application in modern chemical synthesis. This aldehyde compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. In chemical synthesis, 3-Bromo-2,4-difluorobenzaldehyde plays a crucial role as a valuable intermediate for the preparation of diverse organic molecules. Its unique structure containing both bromine and fluorine atoms imparts distinct reactivity and selectivity in the formation of complex molecular structures. One notable application of 3-Bromo-2,4-difluorobenzaldehyde is in the synthesis of heterocyclic compounds, specifically in the construction of biologically active molecules such as pharmaceuticals. The presence of the bromine and difluoromethyl groups in the benzaldehyde scaffold enables the selective functionalization of the aromatic ring, facilitating the synthesis of targeted compounds with enhanced pharmacological properties. Furthermore, this compound is often utilized as a key starting material in metal-catalyzed cross-coupling reactions, carbon-carbon bond formations, and other synthetic transformations that are essential for the assembly of complex organic molecules. Its structural versatility and reactivity make it a valuable tool for synthetic chemists working in various research fields.
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