114498-55-4 | Oxazolo[4,5-c]pyridin-2-amine

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$25.00	$18.00
250mg	98%	in stock	$50.00	$35.00
5g	98%	in stock	$919.00	$644.00

Description

• Catalog Number: AA18667
• Chemical Name: Oxazolo[4,5-c]pyridin-2-amine
• CAS Number: 114498-55-4
• Molecular Formula: C6H5N3O
• Molecular Weight: 135.1234
• MDL Number: MFCD15526655
• SMILES: Nc1nc2c(o1)ccnc2

Computed Properties

• Complexity: 130
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• XLogP3: 0.3

Upstream Synthesis Route

Oxazolo[4,5-c]pyridin-2-amine is a versatile compound widely utilized in chemical synthesis for its unique structural properties and reactivity. As a heterocyclic amine, it serves as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and advanced materials.In organic synthesis, Oxazolo[4,5-c]pyridin-2-amine acts as a key intermediate in the construction of complex molecular frameworks with diverse functionalities. Its presence in the design of new drug candidates often imparts specific biological activities, making it a valuable moiety in medicinal chemistry research.Due to its electron-rich nature and favorable steric profile, Oxazolo[4,5-c]pyridin-2-amine displays pronounced reactivity in a range of transformations including cross-coupling reactions, cyclization processes, and heterocycle functionalization. This reactivity profile allows for efficient and selective modification of the compound, enabling the synthesis of structurally intricate molecules with high precision.Moreover, the presence of the oxazole and pyridine rings in Oxazolo[4,5-c]pyridin-2-amine offers diverse opportunities for diversification through regioselective and stereoselective reactions, leading to the rapid generation of molecular diversity in the development of novel chemical entities.Overall, the strategic incorporation of Oxazolo[4,5-c]pyridin-2-amine in chemical synthesis endeavors offers a powerful approach to accessing valuable structural motifs and expanding the scope of molecular design in diverse scientific disciplines.