2-Thiophenesulfonyl chloride
97%
- Product Code: 239762
Alias:
thiophene-2-sulfonyl chloride; 2-thiophenesulfonyl chloride
CAS:
16629-19-9
Molecular Weight: | 182.65 g./mol | Molecular Formula: | C₄H₃ClO₂S₂ |
---|---|---|---|
EC Number: | 240-677-1 | MDL Number: | MFCD00005426 |
Melting Point: | 30-32 °C(lit.) | Boiling Point: | 130-132 °C14 mm Hg(lit.) |
Density: | Storage Condition: | 2~8°C |
Product Description:
Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of sulfonyl groups into organic molecules, facilitating the creation of sulfonamides, which are common structural motifs in many biologically active compounds. Widely employed in medicinal chemistry for drug development, especially in the design of enzyme inhibitors. Also utilized in the preparation of dyes and functional materials due to its ability to modify aromatic systems. Its role as a sulfonylating agent makes it valuable in both laboratory research and industrial-scale organic transformations.
Product Specification:
Test | Specification |
---|---|
Purity (GC) | 97%-100% |
Purity (Titration with AgNO3) | 96.5%-103.5% |
APPEARANCE | COLORLESS TO YELLOW TO BLUE-GREEN TO BROWN-PURPLE LIQUID OR SOLID |
INFRARED SPECTRUM | Conforms to Structure |
NOTE | This product is low melting point solid, may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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5.000 | 10-20 days | $19.73 |
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25.000 | 10-20 days | $95.02 |
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100.000 | 10-20 days | $301.16 |
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2-Thiophenesulfonyl chloride
Used primarily as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactivity allows for the introduction of sulfonyl groups into organic molecules, facilitating the creation of sulfonamides, which are common structural motifs in many biologically active compounds. Widely employed in medicinal chemistry for drug development, especially in the design of enzyme inhibitors. Also utilized in the preparation of dyes and functional materials due to its ability to modify aromatic systems. Its role as a sulfonylating agent makes it valuable in both laboratory research and industrial-scale organic transformations.
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