1015609-75-2 | 6-Iodo-1h-pyrrolo[3,2-b]pyridine

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$24.00	$17.00
250mg	95%	in stock	$47.00	$33.00
1g	95%	in stock	$109.00	$76.00
5g	95%	in stock	$539.00	$378.00

Description

• Catalog Number: AA05997
• Chemical Name: 6-Iodo-1h-pyrrolo[3,2-b]pyridine
• CAS Number: 1015609-75-2
• Molecular Formula: C7H5IN2
• Molecular Weight: 244.0325
• MDL Number: MFCD09859119
• SMILES: Ic1cnc2c(c1)[nH]cc2

Computed Properties

• Complexity: 129
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• XLogP3: 1.7

Upstream Synthesis Route

6-Iodo-1H-pyrrolo[3,2-b]pyridine is a versatile chemical compound widely used in organic synthesis due to its unique structure and reactivity. This compound is particularly valuable in the field of medicinal chemistry and drug discovery, where it serves as a key building block for the synthesis of various biologically active molecules.One of the notable applications of 6-Iodo-1H-pyrrolo[3,2-b]pyridine is in the preparation of heterocyclic compounds with potential pharmacological properties. By utilizing this building block, chemists can efficiently access diverse libraries of compounds that exhibit promising activities against various disease targets. The iodo substituent in 6-Iodo-1H-pyrrolo[3,2-b]pyridine provides a convenient handle for further functionalization, enabling the introduction of different substituents to modulate the physicochemical and biological properties of the final molecules.Moreover, 6-Iodo-1H-pyrrolo[3,2-b]pyridine can also be employed in cross-coupling reactions to form complex molecular frameworks. Its fused pyrrolopyridine structure allows for the construction of structurally intricate molecules through coupling with different aryl or alkyl partners. This strategy has been successfully applied in the synthesis of natural products, pharmaceuticals, and advanced materials.In summary, the strategic incorporation of 6-Iodo-1H-pyrrolo[3,2-b]pyridine in chemical synthesis enables the efficient assembly of diverse molecular scaffolds with potential applications in drug discovery and material science. Its versatile reactivity and compatibility with various synthetic methodologies make it a valuable tool for organic chemists striving to create novel compounds with enhanced biological activities and functional properties.