1199773-21-1 | 3-Bromo-2-methyl-6-morpholinopyridine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$155.00	$108.00
5g	98%	in stock	$573.00	$402.00
10g	98%	in stock	$946.00	$662.00
25g	98%	in stock	$1,536.00	$1,075.00

Description

• Catalog Number: AA33409
• Chemical Name: 3-Bromo-2-methyl-6-morpholinopyridine
• CAS Number: 1199773-21-1
• Molecular Formula: C10H13BrN2O
• Molecular Weight: 257.1270
• MDL Number: MFCD13195775
• SMILES: Cc1nc(ccc1Br)N1CCOCC1

Computed Properties

• Complexity: 185
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 14
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• XLogP3: 2

Upstream Synthesis Route

The compound 4-(5-Bromo-6-methylpyridin-2-yl)morpholine, also known as $name$, is a versatile building block in chemical synthesis. Its unique structure confers it with the ability to participate in various synthetic reactions, making it a valuable tool for organic chemists.One common application of $name$ in chemical synthesis is as a key intermediate in the production of pharmaceutical compounds. The presence of the bromo and methyl groups on the pyridine ring, combined with the morpholine moiety, allows for selective functionalization and diversification of the molecule. This enables chemists to introduce specific functional groups at precise locations, facilitating the synthesis of complex drug molecules with desired pharmacological properties.Moreover, the presence of the bromo group in 4-(5-Bromo-6-methylpyridin-2-yl)morpholine makes it a useful substrate for transition metal catalyzed cross-coupling reactions. These reactions are widely utilized in modern organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds. By leveraging the unique reactivity of $name$ in such transformations, chemists can access a wide range of structurally diverse compounds efficiently.Additionally, the morpholine functionality in $name$ offers the potential for the formation of heterocyclic structures through intramolecular cyclization reactions. These reactions are crucial for constructing biologically active compounds, natural products, and functional materials.Overall, the versatility of 4-(5-Bromo-6-methylpyridin-2-yl)morpholine in chemical synthesis makes it a valuable tool for medicinal chemistry, material science, and other fields that rely on the precise design and synthesis of complex molecules.