2-Chloro-4-fluorobenzenemethanesulfonamide
95%
- Product Code: 116452
CAS:
1001026-51-2
| Molecular Weight: | 223.65 g./mol | Molecular Formula: | C₇H₇ClFNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11212986 | |
| Melting Point: | Boiling Point: | 372.0±52.0 °C(Predicted) | |
| Density: | 1.525±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry, dark |
Product Description:
This chemical is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure allows it to be incorporated into molecules that target specific enzymes or receptors, making it valuable in the creation of potential drug candidates. It is particularly relevant in the development of anti-inflammatory and antibacterial agents, where its sulfonamide group plays a crucial role in enhancing binding affinity and efficacy. Additionally, it is utilized in organic chemistry laboratories for studying reaction mechanisms and developing novel synthetic pathways. Its halogenated aromatic ring also makes it a useful building block for designing materials with specific electronic or photophysical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €203.96 |
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| 0.250 | 10-20 days | €305.82 |
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| 1.000 | 10-20 days | €764.55 |
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2-Chloro-4-fluorobenzenemethanesulfonamide
This chemical is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure allows it to be incorporated into molecules that target specific enzymes or receptors, making it valuable in the creation of potential drug candidates. It is particularly relevant in the development of anti-inflammatory and antibacterial agents, where its sulfonamide group plays a crucial role in enhancing binding affinity and efficacy. Additionally, it is utilized in organic chemistry laboratories for studying reaction mechanisms and developing novel synthetic pathways. Its halogenated aromatic ring also makes it a useful building block for designing materials with specific electronic or photophysical properties.
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