AB34740
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.
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 |
Complexity: | 114 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 2 |
Rotatable Bond Count: | 1 |
XLogP3: | 2.5 |
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.