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AE11564

107496-54-8 | 3,3-Difluorocyclobutanecarboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $5.00 $4.00 -   +
1g 98% in stock $8.00 $5.00 -   +
5g 98% in stock $19.00 $14.00 -   +
10g 98% in stock $35.00 $24.00 -   +
25g 98% in stock $79.00 $55.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE11564
Chemical Name: 3,3-Difluorocyclobutanecarboxylic acid
CAS Number: 107496-54-8
Molecular Formula: C5H6F2O2
Molecular Weight: 136.0967
MDL Number: MFCD08705857
SMILES: OC(=O)C1CC(C1)(F)F

 

Computed Properties
Complexity: 136  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  
XLogP3: 0.9  

 

 

Upstream Synthesis Route
  • 3,3-Difluorocyclobutanecarboxylic acid is a versatile chemical compound that finds extensive application in chemical synthesis reactions. Due to its unique structure and properties, this compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials.In organic synthesis, 3,3-Difluorocyclobutanecarboxylic acid can be utilized as a key intermediate in the preparation of complex molecules. Its incorporation into the molecular structure of target compounds can impart specific properties or functionalities that are crucial for the desired biological or chemical activity. This compound's fluorinated cyclobutane ring provides steric and electronic effects that can lead to enhanced reactivity and selectivity in synthetic transformations.Moreover, 3,3-Difluorocyclobutanecarboxylic acid serves as a valuable source of fluorine atoms in organic chemistry. The presence of fluorine in organic molecules can dramatically influence their physicochemical properties, such as lipophilicity, metabolic stability, and bioavailability. Therefore, the strategic introduction of difluorocyclobutane moieties using this acid can lead to the development of potent drug candidates or specialty chemicals with improved properties.Overall, the application of 3,3-Difluorocyclobutanecarboxylic acid in chemical synthesis enables chemists to access novel molecular scaffolds and functional groups that are challenging to obtain through traditional methods. By harnessing the unique reactivity and fluorination capabilities of this compound, researchers can innovate in drug discovery, materials science, and other areas of chemical research.
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