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50585-72-3

Fluoromethanesulfonamide

Catalog#: AR01A4ZA  |   CAS#: 50585-72-3  |   MDL#: MFCD28383685  |   MF: CH4FNO2S  |   MW: 113.1114

Packsize Purity Price Availability Quantity
50mg 95% $703.00 2-3 weeks Buy Now Add To Cart
100mg 95% $911.00 2-3 weeks Buy Now Add To Cart
250mg 95% $1,290.00 2-3 weeks Buy Now Add To Cart
500mg 95% $2,018.00 2-3 weeks Buy Now Add To Cart
1g 95% $2,579.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR01A4ZA
Chemical Name Fluoromethanesulfonamide
CAS Number 50585-72-3
Molecular Formula CH4FNO2S
Molecular Weight 113.1114
MDL Number MFCD28383685
SMILES FCS(=O)(=O)N

Fluoromethanesulfonamide is a versatile chemical compound commonly used in chemical synthesis processes. Its unique properties make it a valuable reagent for various applications in the field of organic chemistry.One of the key applications of fluoromethanesulfonamide in chemical synthesis is as a fluorine source in nucleophilic fluorination reactions. Fluorine is a highly valuable atom in organic chemistry due to its small size and high electronegativity, which can significantly impact the reactivity and properties of a molecule. Fluoromethanesulfonamide serves as a stable and readily available source of fluorine, allowing chemists to introduce this important element selectively into a target molecule.Additionally, fluoromethanesulfonamide can act as a mild and efficient fluorinating agent in various chemical transformations, enabling the installation of fluorine atoms in specific positions within a molecule. This capability is particularly useful in pharmaceutical and agrochemical research, where the introduction of fluorine can enhance the biological activity, metabolic stability, and overall properties of a compound.Furthermore, fluoromethanesulfonamide's compatibility with a wide range of functional groups and reaction conditions makes it a valuable tool for synthetic chemists seeking to access fluorinated compounds with precision and control. Its use in synthetic methods such as nucleophilic fluorination, fluorinative cyclization, and fluorinated building block synthesis has enabled the development of novel molecules with diverse applications in drug discovery, materials science, and chemical manufacturing.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
Packing Group -

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