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AA03374

4522-35-4 | 3-Iodopyrazole

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $6.00 $4.00 -   +
1g 98% in stock $8.00 $5.00 -   +
5g 98% in stock $20.00 $14.00 -   +
10g 98% in stock $33.00 $23.00 -   +
25g 98% in stock $56.00 $39.00 -   +
100g 98% in stock $159.00 $111.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA03374
Chemical Name: 3-Iodopyrazole
CAS Number: 4522-35-4
Molecular Formula: C3H3IN2
Molecular Weight: 193.9738
MDL Number: MFCD12022324
SMILES: Ic1cc[nH]n1

 

Computed Properties
Complexity: 48.1  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 6  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 1  
XLogP3: 0.9  

 

 

Upstream Synthesis Route
  • 3-Iodo-1H-pyrazole is a versatile building block in chemical synthesis due to its unique structural properties and reactivity. This compound serves as a powerful nucleophile in organic reactions, allowing for the formation of new carbon-carbon or carbon-heteroatom bonds. In particular, 3-Iodo-1H-pyrazole is commonly used in the synthesis of pharmaceuticals, agrochemicals, and materials.One key application of 3-Iodo-1H-pyrazole is in the preparation of heterocyclic compounds. By reacting with different electrophiles or coupling partners, this compound can be utilized to introduce the pyrazole ring motif into molecular structures. This enables the modulation of biological activity or tuning of physical properties in target molecules.In addition, 3-Iodo-1H-pyrazole can participate in metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura or Stille couplings, leading to the formation of complex organic frameworks. These reactions offer a powerful means to construct carbon-carbon bonds efficiently and selectively, facilitating the synthesis of structurally diverse compounds.Furthermore, 3-Iodo-1H-pyrazole is valued for its role as a halogenated building block, enabling further functionalization through substitution or elimination reactions. This flexibility in chemical modifications broadens the scope of synthetic routes and provides access to a wide range of derivatives with tailored properties.Overall, the strategic use of 3-Iodo-1H-pyrazole in chemical synthesis offers synthetic chemists a versatile tool for designing and accessing novel molecules with potential applications in various fields of chemistry and beyond.
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