1190317-82-8 | 5-Bromo-1H-pyrrolo[3,2-b]pyridine-3-carbaldehyde

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	1 week	$134.00	$94.00
250mg	98%	1 week	$227.00	$159.00
1g	98%	1 week	$611.00	$428.00

Description

• Catalog Number: AA22847
• Chemical Name: 5-Bromo-1H-pyrrolo[3,2-b]pyridine-3-carbaldehyde
• CAS Number: 1190317-82-8
• Molecular Formula: C8H5BrN2O
• Molecular Weight: 225.0421
• MDL Number: MFCD12962975
• SMILES: O=Cc1c[nH]c2c1nc(Br)cc2

Upstream Synthesis Route

5-Bromo-1H-pyrrolo[3,2-b]pyridine-3-carboxaldehyde is a versatile compound that finds wide applications in chemical synthesis. Due to its unique structure and reactivity, this compound serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and organic materials.In synthetic chemistry, 5-Bromo-1H-pyrrolo[3,2-b]pyridine-3-carboxaldehyde is commonly used as a key intermediate in the synthesis of heterocyclic compounds. Its bromo substituent allows for further functionalization through various reactions such as Suzuki coupling, Heck reaction, and Sonogashira coupling, enabling the introduction of different functional groups and modifications.Moreover, the aldehyde group in 5-Bromo-1H-pyrrolo[3,2-b]pyridine-3-carboxaldehyde serves as a reactive site for diverse transformations such as aldol condensation, Grignard reaction, and reductive amination. This reactivity opens up avenues for the construction of complex molecular structures and the formation of carbon-carbon and carbon-heteroatom bonds in organic synthesis.Overall, the strategic incorporation of 5-Bromo-1H-pyrrolo[3,2-b]pyridine-3-carboxaldehyde in chemical reactions facilitates the efficient assembly of diverse molecules with intricate architectures, making it an indispensable tool for synthetic chemists seeking to access novel compounds with potential biological or material applications.