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51270-36-1

1-Bromo-N-tert-butylmethanesulfonamide

Catalog#: AR01BD17  |   CAS#: 51270-36-1  |   MDL#: MFCD00460681  |   MF: C5H12BrNO2S  |   MW: 230.1233

Packsize Purity Price Availability Quantity
50mg 95% $307.00 2-3 weeks Buy Now Add To Cart
100mg 95% $446.00 2-3 weeks Buy Now Add To Cart
250mg 95% $628.00 2-3 weeks Buy Now Add To Cart
500mg 95% $976.00 2-3 weeks Buy Now Add To Cart
1g 95% $1,241.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR01BD17
Chemical Name 1-Bromo-N-tert-butylmethanesulfonamide
CAS Number 51270-36-1
Molecular Formula C5H12BrNO2S
Molecular Weight 230.1233
MDL Number MFCD00460681
SMILES BrCS(=O)(=O)NC(C)(C)C

1-Bromo-N-(1,1-dimethylethyl)methanesulfonamide is a versatile chemical compound widely employed in organic synthesis due to its unique reactivity and functional group compatibility. This compound serves as a valuable reagent in various chemical transformations, particularly in the preparation of sulfonyl and sulfonamide derivatives.In chemical synthesis, 1-Bromo-N-(1,1-dimethylethyl)methanesulfonamide is utilized as a selective source of the sulfonyl functional group. Its bromide moiety allows for facile substitution reactions, enabling the introduction of the sulfonyl group onto a wide range of organic molecules. This reagent is particularly useful in the synthesis of sulfonamide compounds, which are important intermediates in pharmaceuticals, agrochemicals, and materials science.Moreover, the tert-butyl substituent on the sulfonamide nitrogen enhances the stability and selectivity of reactions involving this compound. The steric hindrance provided by the tert-butyl group helps to control the regioselectivity and stereochemistry of the sulfonamide formation, making it a valuable tool in complex molecule synthesis.Overall, 1-Bromo-N-(1,1-dimethylethyl)methanesulfonamide offers chemists a versatile and reliable reagent for the construction of sulfonamide derivatives with high efficiency and selectivity. Its unique structural features and reactivity profile make it an essential building block in modern organic synthesis strategies.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
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