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Home  > Chemistry  > Organic Building Blocks  > Difluoromethyls  > 5-Chloro-3-(difluoromethyl)-1-methyl-1h-pyrazole-4-carboxylic acid

AE10958

1202993-11-0 | 5-Chloro-3-(difluoromethyl)-1-methyl-1h-pyrazole-4-carboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $12.00 $9.00 -   +
1g 97% in stock $27.00 $19.00 -   +
5g 97% in stock $100.00 $70.00 -   +
10g 97% in stock $200.00 $140.00 -   +
25g 97% in stock $429.00 $301.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE10958
Chemical Name: 5-Chloro-3-(difluoromethyl)-1-methyl-1h-pyrazole-4-carboxylic acid
CAS Number: 1202993-11-0
Molecular Formula: C6H5ClF2N2O2
Molecular Weight: 210.5659064
MDL Number: MFCD12827693
SMILES: FC(c1nn(c(c1C(=O)O)Cl)C)F

 

Computed Properties
Complexity: 217  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 1.4  

 

 

Upstream Synthesis Route
  • 5-Chloro-3-(difluoromethyl)-1-methyl-1H-pyrazole-4-carboxylic acid plays a crucial role in chemical synthesis as a versatile building block. Its unique structure allows it to be used in the creation of various pharmaceutical, agrochemical, and material science compounds. Due to the presence of the chloro, difluoromethyl, and carboxylic acid functional groups, this compound can participate in a wide range of chemical reactions, including nucleophilic substitution, condensation, and complexation reactions. Its application in organic synthesis enables the formation of diverse molecular structures with potential biological activity or material properties. Additionally, the presence of the pyrazole ring in the molecule enhances its reactivity and can lead to the development of novel derivatives with tailored properties.
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