1033610-45-5 | 4-Bromo-3,5-dimethoxypyridine

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$28.00	$19.00
250mg	98%	in stock	$43.00	$30.00
1g	98%	in stock	$90.00	$63.00

Description

• Catalog Number: AD80619
• Chemical Name: 4-Bromo-3,5-dimethoxypyridine
• CAS Number: 1033610-45-5
• Molecular Formula: C7H8BrNO2
• Molecular Weight: 218.0479
• MDL Number: MFCD14705143
• SMILES: COc1cncc(c1Br)OC

Computed Properties

• Complexity: 111
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• XLogP3: 1.5

Upstream Synthesis Route

4-Bromo-3,5-dimethoxypyridine is a versatile compound widely utilized in chemical synthesis for its unique reactivity and structural properties. This compound serves as a valuable building block in the development of various pharmaceuticals, agrochemicals, and organic materials. In organic synthesis, 4-Bromo-3,5-dimethoxypyridine can be used as a key intermediate in the preparation of heterocyclic compounds, which are essential in the creation of diverse chemical structures with specific functionalities.One of the key applications of 4-Bromo-3,5-dimethoxypyridine in chemical synthesis is its role as a versatile electrophilic reagent. Due to the presence of the bromine atom and methoxy groups, this compound can undergo various substitution reactions to introduce functional groups at specific positions on the pyridine ring. These reactions allow for the modification of the molecular structure to fine-tune the properties of the final product, making 4-Bromo-3,5-dimethoxypyridine an invaluable tool in the design and synthesis of complex organic molecules.Moreover, 4-Bromo-3,5-dimethoxypyridine can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds with aryl or vinyl boronic acids. This strategy enables the incorporation of aryl or vinyl substituents into the pyridine ring, expanding the chemical diversity and functional group tolerance of the final product. Additionally, the presence of methoxy groups in 4-Bromo-3,5-dimethoxypyridine can provide steric and electronic effects that influence the regioselectivity and reactivity of subsequent transformations, making it a valuable scaffold for molecular design in chemical synthesis.Overall, 4-Bromo-3,5-dimethoxypyridine plays a crucial role in advancing the field of chemical synthesis by offering a robust platform for the construction of complex organic molecules with tailored properties and functionalities. Its diverse applications and synthetic utility make it a valuable asset in the toolkit of synthetic chemists seeking to explore new avenues in drug discovery, material science, and molecular design.