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AB89538

89717-64-6 | 4-Bromo-3-nitro-1h-pyrazole

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $10.00 $7.00 -   +
250mg 97% in stock $12.00 $8.00 -   +
1g 97% in stock $14.00 $10.00 -   +
5g 97% in stock $42.00 $30.00 -   +
10g 97% in stock $84.00 $59.00 -   +
25g 97% in stock $198.00 $139.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB89538
Chemical Name: 4-Bromo-3-nitro-1h-pyrazole
CAS Number: 89717-64-6
Molecular Formula: C3H2BrN3O2
Molecular Weight: 191.97087999999997
MDL Number: MFCD01114992
SMILES: [O-][N+](=O)c1n[nH]cc1Br

 

Computed Properties
Complexity: 125  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.1  

 

 

Upstream Synthesis Route
  • 4-Bromo-3-nitro-1H-pyrazole is a versatile chemical compound that finds wide application in chemical synthesis. This compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and other organic compounds. Its unique structure and reactivity make it an important intermediate in the synthesis of heterocyclic compounds.In chemical synthesis, 4-Bromo-3-nitro-1H-pyrazole is often utilized as a key starting material for the construction of more complex molecules. It can undergo various transformation reactions, such as substitution, reduction, and functional group interconversion, to introduce desired functionalities into the final product. Additionally, its nitro and bromo substituents provide sites for further derivatization, allowing chemists to modify the compound in a controlled manner.The presence of both the nitro and bromo groups in 4-Bromo-3-nitro-1H-pyrazole make it particularly useful in transition metal catalyzed cross-coupling reactions. These reactions enable the formation of carbon-carbon and carbon-heteroatom bonds, facilitating the creation of structurally diverse compounds with improved properties. By incorporating 4-Bromo-3-nitro-1H-pyrazole into synthetic pathways, chemists can access a wide range of derivatives for various applications in the pharmaceutical, agrochemical, and materials science fields.
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