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60965-56-2

3-Furansulfonyl chloride, 2-methyl-

Catalog#: AR01IF3E  |   CAS#: 60965-56-2  |   MDL#: MFCD19201250  |   MF: C5H5ClO3S  |   MW: 180.6094

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 AR01IF3E
Chemical Name 3-Furansulfonyl chloride, 2-methyl-
CAS Number 60965-56-2
Molecular Formula C5H5ClO3S
Molecular Weight 180.6094
MDL Number MFCD19201250
SMILES Cc1occc1S(=O)(=O)Cl

3-Furansulfonyl chloride, 2-methyl- is a versatile building block in chemical synthesis due to its unique reactivity and functional group compatibility. This compound serves as a valuable tool for chemists in various applications, such as:1. As a acylating agent: 3-Furansulfonyl chloride, 2-methyl- exhibits acyl chloride reactivity, allowing it to be utilized in acylation reactions with nucleophiles such as amines, alcohols, and thiols. This enables the introduction of the 3-furansulfonyl group onto a wide range of organic molecules, making it a useful tool for structural modification and functionalization.2. As a sulfonylating agent: The sulfonyl chloride functionality of 3-Furansulfonyl chloride, 2-methyl- can be activated in the presence of suitable nucleophiles, leading to the formation of sulfonyl derivatives. These derivatives are valuable intermediates in the synthesis of pharmaceuticals, agrochemicals, and materials with desired properties.3. In heterocycle synthesis: The furan ring in 3-Furansulfonyl chloride, 2-methyl- can participate in various cycloaddition reactions and cascade processes, allowing for the construction of complex heterocyclic structures. This compound can serve as a key building block in the synthesis of biologically active compounds and natural products.Overall, 3-Furansulfonyl chloride, 2-methyl- is a valuable reagent in organic synthesis, offering chemists a powerful tool for the efficient construction of diverse molecular frameworks with precise control over functional group placement and stereochemistry.
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