1146290-19-8 | 5-Bromo-2-chloropyridine-3-sulfonyl chloride

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$267.00	$187.00
1g	95%	in stock	$674.00	$472.00
5g	95%	in stock	$1,996.00	$1,397.00

Description

• Catalog Number: AE48159
• Chemical Name: 5-Bromo-2-chloropyridine-3-sulfonyl chloride
• CAS Number: 1146290-19-8
• Molecular Formula: C5H2BrCl2NO2S
• Molecular Weight: 290.9499
• MDL Number: MFCD11858018
• SMILES: Brc1cnc(c(c1)S(=O)(=O)Cl)Cl

Computed Properties

• Complexity: 253
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• XLogP3: 2.5

Upstream Synthesis Route

5-Bromo-2-chloropyridine-3-sulfonyl chloride, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. As a sulfonyl chloride derivative of pyridine, $name$ serves as a valuable building block in the creation of numerous complex organic molecules. Its inherent reactivity makes it particularly valuable in the field of medicinal chemistry and pharmaceutical research, where precise and efficient synthesis routes are essential for drug discovery and development.One of the key applications of 5-Bromo-2-chloropyridine-3-sulfonyl chloride is as a sulfonylation reagent in various synthetic reactions. By utilizing its sulfonyl chloride functional group, chemists can introduce sulfonyl moieties into target molecules, enabling the modification of their physicochemical properties and biological activities. This ability to functionalize organic molecules with sulfonyl groups is crucial in the design and construction of novel compounds with desired properties for applications in drug development.Moreover, the presence of both bromo and chloro substituents on the pyridine ring of $name$ offers additional synthetic flexibility. These groups can serve as handles for further derivatization, enabling the introduction of diverse functional groups and the creation of structurally diverse chemical libraries for screening in drug discovery programs. The unique combination of reactivity and substituent diversity makes 5-Bromo-2-chloropyridine-3-sulfonyl chloride a valuable tool for synthetic chemists working in the pharmaceutical and agrochemical industries.