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71703-15-6

2-(3-Bromophenyl)isothiazolidine 1,1-dioxide

Catalog#: AR00645L  |   CAS#: 71703-15-6  |   MDL#: MFCD09933299  |   MF: C9H10BrNO2S  |   MW: 276.1502

Packsize Purity Price Availability Quantity
100mg 98% $21.00 Global Stock Buy Now Add To Cart
250mg 98% $34.00 Global Stock Buy Now Add To Cart
1g 98% $69.00 Global Stock Buy Now Add To Cart
5g 98% $204.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00645L
Chemical Name 2-(3-Bromophenyl)isothiazolidine 1,1-dioxide
CAS Number 71703-15-6
Molecular Formula C9H10BrNO2S
Molecular Weight 276.1502
MDL Number MFCD09933299
SMILES Brc1cccc(c1)N1CCCS1(=O)=O

2-(3-Bromophenyl)isothiazolidine 1,1-dioxide, also known as $name$, is a versatile compound widely used in chemical synthesis. Its primary application lies in organic chemistry, where it serves as a key building block for the synthesis of various pharmaceuticals, agrochemicals, and materials. One common use of $name$ is as a valuable intermediate in the production of heterocyclic compounds, particularly in the formation of diverse pharmaceutical agents. Its unique structure and reactivity make it ideal for facilitating complex organic reactions, such as cyclizations and cross-coupling reactions, leading to the efficient synthesis of novel molecules with potential therapeutic applications.Additionally, $name$ can act as a potent electrophilic reagent in various transformations, enabling the introduction of the 3-bromophenyl group into target molecules. This functionality is crucial for the modification of organic scaffolds and the design of new chemical entities with desired properties.Furthermore, in material science, 2-(3-Bromophenyl)isothiazolidine 1,1-dioxide finds utility in the development of advanced polymers and functional materials. Its incorporation into polymer matrices imparts specific chemical and physical properties, enhancing the performance and functionality of the resulting materials in various applications, such as coatings, adhesives, and electronic devices. Overall, the strategic incorporation of $name$ in chemical synthesis enables researchers to access a diverse array of molecular structures, opening up new avenues for drug discovery, materials science, and other areas of research and development.
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GHS Pictogram N/A
UN# -
Hazard Statements -
Class -
Packing Group -

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