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Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > 1,4,6,7-Tetrahydro-3-(trifluoromethyl)pyrano-[4,3-c]-pyrazole

AA09044

1022931-45-8 | 1,4,6,7-Tetrahydro-3-(trifluoromethyl)pyrano-[4,3-c]-pyrazole

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $19.00 $14.00 -   +
1g 97% in stock $173.00 $121.00 -   +
5g 97% in stock $713.00 $499.00 -   +
10g 97% in stock $1,179.00 $825.00 -   +
25g 97% in stock $2,112.00 $1,479.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA09044
Chemical Name: 1,4,6,7-Tetrahydro-3-(trifluoromethyl)pyrano-[4,3-c]-pyrazole
CAS Number: 1022931-45-8
Molecular Formula: C7H7F3N2O
Molecular Weight: 192.1385
MDL Number: MFCD08447340
SMILES: FC(c1n[nH]c2c1COCC2)(F)F

 

Computed Properties
Complexity: 197  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
XLogP3: 0.9  

 

 

Upstream Synthesis Route
  • 3-(Trifluoromethyl)-1,4,6,7-tetrahydropyrano[4,3-c]pyrazole is a versatile compound commonly utilized in chemical synthesis for its unique structure and valuable reactivity. This compound serves as a key building block in the formation of complex organic molecules, particularly in the field of medicinal chemistry and drug development. Its functional groups and cyclic structure make it a valuable intermediate in the synthesis of biologically active compounds and pharmaceuticals. The trifluoromethyl group enhances the compound's lipophilicity and can influence its pharmacokinetic properties. Additionally, the fused pyrano-pyrazole ring system provides rigidity and specificity to the molecules synthesized using this compound, potentially leading to enhanced biological activity.In chemical synthesis, 3-(Trifluoromethyl)-1,4,6,7-tetrahydropyrano[4,3-c]pyrazole can participate in a variety of reactions, including functional group transformations, cyclizations, and heterocyclic ring formations. Its presence in the molecular structure can introduce desirable properties such as increased stability, improved binding affinity, and enhanced metabolic resistance.Overall, the strategic incorporation of 3-(Trifluoromethyl)-1,4,6,7-tetrahydropyrano[4,3-c]pyrazole in chemical synthesis enables the construction of diverse and pharmacologically relevant compounds with the potential for application in drug discovery and development.
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