1171919-00-8 | 2-Chloro-3,5-diiodo-4-pyridinamine

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$53.00	$38.00
10g	95%	in stock	$94.00	$66.00

Description

• Catalog Number: AA17806
• Chemical Name: 2-Chloro-3,5-diiodo-4-pyridinamine
• CAS Number: 1171919-00-8
• Molecular Formula: C5H3ClI2N2
• Molecular Weight: 380.3527
• MDL Number: MFCD12498707
• SMILES: Ic1cnc(c(c1N)I)Cl

Computed Properties

• Complexity: 124
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: 2.4

Upstream Synthesis Route

2-Chloro-3,5-diiodopyridin-4-amine is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the development of various organic molecules due to its strategic positioning of halogen and amine functional groups. In chemical synthesis, 2-Chloro-3,5-diiodopyridin-4-amine can act as a key intermediate in the creation of pharmaceuticals, agrochemicals, and materials. The presence of both chloro and iodo substituents on the pyridine ring allows for selective cross-coupling reactions, enabling the formation of complex structures with high regioselectivity. Additionally, the amine group can serve as a point for further derivatization, expanding the compound's utility in synthetic pathways.Furthermore, the unique electronic properties of 2-Chloro-3,5-diiodopyridin-4-amine make it a valuable candidate for the development of functional materials such as organic semiconductors and dyes. Its electron-rich nature combined with the halogen substituents offer opportunities for tailored tuning of properties, making it a versatile tool in material science research.Overall, 2-Chloro-3,5-diiodopyridin-4-amine plays a crucial role in chemical synthesis by enabling the construction of diverse molecular structures with precision and efficiency. Its broad applications in pharmaceuticals, agrochemicals, and materials highlight its significance in the realm of organic chemistry and synthetic methodology.