108966-71-8 | 3,4-Difluorobenzenesulfonamide

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$14.00	$10.00
1g	97%	in stock	$23.00	$16.00
5g	97%	in stock	$58.00	$41.00
10g	97%	in stock	$90.00	$63.00
25g	97%	in stock	$112.00	$78.00
100g	97%	in stock	$329.00	$230.00

Description

• Catalog Number: AB63705
• Chemical Name: 3,4-Difluorobenzenesulfonamide
• CAS Number: 108966-71-8
• Molecular Formula: C6H5F2NO2S
• Molecular Weight: 193.1712
• MDL Number: MFCD00728800
• SMILES: Fc1ccc(cc1F)S(=O)(=O)N

Computed Properties

• Complexity: 249
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 0.9

Upstream Synthesis Route

3,4-Difluorobenzenesulfonamide, also known as $name$, is a valuable compound widely used in chemical synthesis due to its unique properties and versatile applications. In organic chemistry, 3,4-Difluorobenzenesulfonamide serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and advanced materials. Its fluoro-substituted benzene ring imparts enhanced reactivity and stability, making it particularly useful in the synthesis of complex molecules.One prominent application of 3,4-Difluorobenzenesulfonamide is in the formation of sulfonamide derivatives, a class of compounds known for their diverse biological activities and structural motifs. By serving as a sulfonamide precursor, this compound enables the introduction of the sulfonamide functional group into target molecules, facilitating the development of new drug candidates and bioactive compounds. Additionally, the presence of fluorine atoms in 3,4-Difluorobenzenesulfonamide can influence the physicochemical properties of the resulting products, such as lipophilicity and binding affinity, making it an attractive choice for medicinal chemistry research.Furthermore, 3,4-Difluorobenzenesulfonamide can participate in various synthetic transformations, including nucleophilic aromatic substitution, metal-catalyzed coupling reactions, and functional group interconversions. Its versatile reactivity and compatibility with a wide range of reaction conditions make it a valuable tool for chemists seeking to introduce sulfonamide functionality or fluorine substitution into their target molecules. By incorporating 3,4-Difluorobenzenesulfonamide into their synthetic strategies, researchers can access novel compounds with tailored properties and potential applications in drug discovery, material science, and other fields of chemical research.