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AB48752

653-37-2 | Pentafluorobenzaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
1g 98% in stock $12.00 $8.00 -   +
5g 98% in stock $23.00 $16.00 -   +
10g 98% in stock $29.00 $21.00 -   +
25g 98% in stock $70.00 $49.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB48752
Chemical Name: Pentafluorobenzaldehyde
CAS Number: 653-37-2
Molecular Formula: C7HF5O
Molecular Weight: 196.0743
MDL Number: MFCD09032441
SMILES: O=Cc1c(F)c(F)c(c(c1F)F)F
NSC Number: 96967

 

Computed Properties
Complexity: 183  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 6  
Rotatable Bond Count: 1  
XLogP3: 1.9  

 

 

Upstream Synthesis Route
  • **2,3,4,5,6-Pentafluorobenzaldehyde in Chemical Synthesis**In the realm of chemical synthesis, 2,3,4,5,6-Pentafluorobenzaldehyde plays a significant role as a versatile building block. This compound, with its unique structure and reactivity, is prized for its ability to participate in a wide array of organic transformations, making it a valuable resource for creating complex molecules in the laboratory.One of the key applications of 2,3,4,5,6-Pentafluorobenzaldehyde is its use as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its electron-withdrawing pentafluorophenyl group imparts enhanced reactivity and selectivity in numerous reactions, making it an attractive starting material for the preparation of advanced drug candidates and crop protection agents.Furthermore, 2,3,4,5,6-Pentafluorobenzaldehyde finds utility in metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura and Heck couplings, enabling the construction of carbon-carbon and carbon-heteroatom bonds with precision. This compound's exceptional stability and compatibility with diverse synthetic methodologies make it an indispensable component in the toolkit of modern organic chemists.Moreover, the presence of five fluorine atoms in 2,3,4,5,6-Pentafluorobenzaldehyde confers unique properties that can be leveraged for the synthesis of fluorinated compounds. These fluorinated motifs are highly sought after in medicinal chemistry and material science due to their distinct pharmacological activities and physical characteristics.In essence, the strategic incorporation of 2,3,4,5,6-Pentafluorobenzaldehyde into synthetic routes opens up a realm of possibilities for the construction of novel molecules with enhanced functionalities and diverse applications across various scientific disciplines.
Literature
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