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633328-88-8

3-Bromo-1H-pyrazolo[4,3-c]pyridine

Catalog#: AR00EDL4  |   CAS#: 633328-88-8  |   MDL#: MFCD11518973  |   MF: C6H4BrN3  |   MW: 198.0201

Packsize Purity Price Availability Quantity
100mg 97% $7.00 Global Stock Buy Now Add To Cart
250mg 97% $15.00 Global Stock Buy Now Add To Cart
1g 97% $51.00 Global Stock Buy Now Add To Cart
5g 97% $250.00 Global Stock Buy Now Add To Cart
10g 97% $403.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00EDL4
Chemical Name 3-Bromo-1H-pyrazolo[4,3-c]pyridine
CAS Number 633328-88-8
Molecular Formula C6H4BrN3
Molecular Weight 198.0201
MDL Number MFCD11518973
SMILES Brc1n[nH]c2c1cncc2

3-Bromo-1H-pyrazolo[4,3-c]pyridine is a versatile chemical compound widely used in chemical synthesis due to its unique properties. This compound serves as a valuable building block in the development and production of various pharmaceuticals, agrochemicals, and materials.1. Ligand Synthesis:
3-Bromo-1H-pyrazolo[4,3-c]pyridine is frequently employed as a ligand in organometallic chemistry. Its ability to coordinate with transition metals enables the formation of stable metal complexes, which are essential in catalyzing a wide range of reactions in organic synthesis. These metal-ligand complexes enhance reaction selectivity and efficiency, making them valuable tools in the development of new chemical compounds.2. Heterocyclic Compound Synthesis:
The presence of both pyrazole and pyridine rings in 3-Bromo-1H-pyrazolo[4,3-c]pyridine makes it a key intermediate for the synthesis of diverse heterocyclic compounds. Through functionalization and derivatization, this compound can be modified to introduce specific functional groups or structural motifs, enabling the creation of novel molecules with targeted properties. These heterocyclic compounds find applications in medicinal chemistry, agrochemical development, and materials science.3. Cross-Coupling Reactions:
3-Bromo-1H-pyrazolo[4,3-c]pyridine is often utilized as a substrate in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions. By reacting with suitable coupling partners, this compound can undergo C–C or C–heteroatom bond formation, leading to the synthesis of complex molecules with varying substitution patterns. These cross-coupling reactions play a crucial role in the construction of molecular scaffolds for drug discovery, material design, and related fields.In summary, 3-Bromo-1H-pyrazolo[4,3-c]pyridine is a valuable reagent in chemical synthesis, offering a wide range of applications in ligand synthesis, heterocyclic compound formation, and cross-coupling reactions. Its versatility and reactivity make it an indispensable tool for researchers and chemists working towards developing innovative compounds with diverse functionalities and applications.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H317-H319
Precautionary Statements P280-P305+P351+P338
Class -
Packing Group -

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