2-Fluoro-4-nitrobenzene-1-sulfonyl chloride
97%
- Product Code: 79154
CAS:
1146290-36-9
| Molecular Weight: | 239.61 g./mol | Molecular Formula: | C₆H₃ClFNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11858095 | |
| Melting Point: | Boiling Point: | 338.2±27.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
Used primarily as a reagent in organic synthesis, this chemical is valuable for introducing sulfonyl groups into molecules, facilitating the creation of sulfonamides and sulfonate esters. It is particularly useful in pharmaceutical research for modifying drug candidates to enhance their biological activity or solubility. Additionally, it serves as an intermediate in the production of dyes, agrochemicals, and specialty chemicals, where its nitro and sulfonyl functionalities enable diverse chemical transformations. Its application in peptide chemistry is also notable, as it aids in protecting amino groups during synthesis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to orange to Brown Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿950.00 |
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| 0.250 | 10-20 days | ฿2,360.00 |
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| 1.000 | 10-20 days | ฿6,100.00 |
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| 5.000 | 10-20 days | ฿29,430.00 |
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2-Fluoro-4-nitrobenzene-1-sulfonyl chloride
Used primarily as a reagent in organic synthesis, this chemical is valuable for introducing sulfonyl groups into molecules, facilitating the creation of sulfonamides and sulfonate esters. It is particularly useful in pharmaceutical research for modifying drug candidates to enhance their biological activity or solubility. Additionally, it serves as an intermediate in the production of dyes, agrochemicals, and specialty chemicals, where its nitro and sulfonyl functionalities enable diverse chemical transformations. Its application in peptide chemistry is also notable, as it aids in protecting amino groups during synthesis.
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