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AB34740

286947-03-3 | 5-Bromo-2-chloro-3-methoxypyridine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $16.00 $11.00 -   +
1g 98% in stock $16.00 $12.00 -   +
5g 98% in stock $79.00 $56.00 -   +
10g 98% in stock $149.00 $105.00 -   +
25g 98% in stock $357.00 $250.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB34740
Chemical Name: 5-Bromo-2-chloro-3-methoxypyridine
CAS Number: 286947-03-3
Molecular Formula: C6H5BrClNO
Molecular Weight: 222.467
MDL Number: MFCD08234976
SMILES: COc1cc(Br)cnc1Cl

 

Computed Properties
Complexity: 114  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 1  
XLogP3: 2.5  

 

 

Upstream Synthesis Route
  • 5-Bromo-2-chloro-3-methoxypyridine is a valuable building block in chemical synthesis due to its versatile reactivity and unique structural properties. This compound is commonly utilized as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its functional groups enable it to participate in a wide range of chemical reactions, making it a valuable tool for organic chemists in designing and creating new compounds.In organic synthesis, 5-Bromo-2-chloro-3-methoxypyridine can serve as a halogenated pyridine building block for the construction of complex molecules. Its halogen substituents can undergo diverse transformations such as Suzuki-Miyaura coupling, Heck reaction, and cross-coupling reactions, allowing for the introduction of different functional groups at specific positions within the pyridine ring. Additionally, the methoxy group provides a handle for further derivatization and modification, expanding the compound's synthetic utility.Furthermore, this compound can act as a valuable precursor for the synthesis of biologically active compounds, including pharmaceutical intermediates and herbicidal agents. Its structural features make it a versatile starting material for the development of new drug candidates with potential therapeutic applications. By leveraging the reactivity of 5-Bromo-2-chloro-3-methoxypyridine in strategic synthetic transformations, chemists can access a diverse array of novel compounds with tailored properties and functionalities.
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