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Home  > Chemistry  > Heterocyclic Building Blocks  > Piperidines  > 1-Benzyl-3,3-difluoro-4,4-piperidinediol

AE16744

1067914-81-1 | 1-Benzyl-3,3-difluoro-4,4-piperidinediol

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $30.00 $21.00 -   +
1g 98% in stock $42.00 $30.00 -   +
5g 98% in stock $116.00 $81.00 -   +
25g 98% in stock $479.00 $335.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE16744
Chemical Name: 1-Benzyl-3,3-difluoro-4,4-piperidinediol
CAS Number: 1067914-81-1
Molecular Formula: C12H15F2NO2
Molecular Weight: 243.2498
MDL Number: MFCD20926176
SMILES: OC1(O)CCN(CC1(F)F)Cc1ccccc1

 

Computed Properties
Complexity: 265  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  
XLogP3: 1.2  

 

 

Upstream Synthesis Route
  • 1-Benzyl-3,3-difluoropiperidine-4,4-diol is a versatile compound that finds widespread application in chemical synthesis as a key building block. With its unique structure and properties, this compound serves as a valuable intermediate in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its strategic placement of functional groups allows for efficient manipulation in synthetic pathways, enabling the synthesis of complex molecules with high efficiency and selectivity. In particular, the presence of the difluoromethyl substituents provides an opportunity for introducing fluorine atoms into target molecules, which can significantly enhance their biological activity or physicochemical properties. Furthermore, the benzyl group offers a handle for further derivatization, enabling the introduction of additional functionalities to tailor the compound for specific applications. Overall, the utilization of 1-Benzyl-3,3-difluoropiperidine-4,4-diol in chemical synthesis showcases its importance as a versatile building block for the efficient and strategic construction of diverse molecular scaffolds with potential utility in various fields.
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