1221398-11-3 | 6-Chloro-5-iodopyridin-2-amine

Packsize	Purity	Availability	Price	Discounted Price
100mg	96%	in stock	$13.00	$9.00
250mg	96%	in stock	$17.00	$12.00
1g	96%	in stock	$20.00	$14.00
5g	96%	in stock	$75.00	$52.00
10g	96%	in stock	$121.00	$85.00
100g	96%	in stock	$1,007.00	$705.00

Description

• Catalog Number: AA55306
• Chemical Name: 6-Chloro-5-iodopyridin-2-amine
• CAS Number: 1221398-11-3
• Molecular Formula: C5H4ClIN2
• Molecular Weight: 254.45613
• MDL Number: MFCD20486991
• SMILES: Nc1ccc(c(n1)Cl)I

Computed Properties

• Complexity: 101
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• XLogP3: 2.1

Upstream Synthesis Route

6-Chloro-5-iodopyridin-2-amine, often referred to as $name$, is a valuable chemical compound widely utilized in chemical synthesis. This compound is a versatile building block in organic chemistry due to its unique structure and reactivity. Its application in chemical synthesis includes being used as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials.One of the primary roles of 6-Chloro-5-iodopyridin-2-amine in chemical synthesis is in the formation of complex heterocyclic compounds. Its presence in a molecule can facilitate the synthesis of diverse pyridine derivatives and other nitrogen-containing heterocycles. Additionally, this compound serves as a crucial precursor in the development of novel pharmaceutical agents and biologically active molecules.Furthermore, 6-Chloro-5-iodopyridin-2-amine is instrumental in the construction of molecular libraries for drug discovery purposes. Its ability to undergo various chemical reactions, such as cross-coupling reactions and substitution reactions, enables the creation of structurally diverse compounds with potential medicinal properties.In summary, the strategic incorporation of 6-Chloro-5-iodopyridin-2-amine in chemical synthesis processes offers researchers and chemists a powerful tool for designing and accessing a wide range of organic molecules with therapeutic and industrial significance.