10168-60-2 | 4-Bromo-3-ethylpyridine hydrobromide

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Description

• Catalog Number: AA06539
• Chemical Name: 4-Bromo-3-ethylpyridine hydrobromide
• CAS Number: 10168-60-2
• Molecular Formula: C7H8BrN
• Molecular Weight: 186.0491
• MDL Number: MFCD19543895
• SMILES: CCc1cnccc1Br

Computed Properties

• Complexity: 85
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.3

Upstream Synthesis Route

4-Bromo-3-ethylpyridine is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. This specific derivative of pyridine serves as a valuable building block in the development of various pharmaceuticals, agrochemicals, and other fine chemicals. Its bromine and ethyl substituents enhance the molecule's compatibility with a wide range of reaction conditions, making it a popular choice for organic chemists seeking to introduce specific functionalities into their target molecules. In particular, 4-Bromo-3-ethylpyridine can be readily employed in transition metal-catalyzed cross-coupling reactions to form complex carbon-carbon and carbon-heteroatom bonds. This allows for the efficient creation of structurally diverse compounds with improved biological or chemical properties. Additionally, its presence in the backbone of certain molecules can influence their physicochemical properties, such as solubility, stability, and binding affinity, making it an essential tool for drug discovery and material science research. Furthermore, the versatile nature of 4-Bromo-3-ethylpyridine enables chemists to explore various synthetic pathways, including nucleophilic substitutions, palladium-catalyzed transformations, and functional group interconversions. Overall, the strategic incorporation of 4-Bromo-3-ethylpyridine into synthetic schemes provides chemists with a valuable tool for the efficient and precise construction of complex molecular architectures with tailored functionalities.