4-(Trifluoromethyl)benzene-1-sulfonyl chloride
98%
- Product Code: 46762
Alias:
p-Trifluoromethylbenzenesulfonyl chloride
CAS:
2991-42-6
Properties:
lumpy solid
Molecular Weight: | 244.62 g./mol | Molecular Formula: | C₇H₄ClF₃O₂S |
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EC Number: | MDL Number: | MFCD00042422 | |
Melting Point: | 30-34 °C | Boiling Point: | 76 °C |
Density: | 1.532 g/cm3 | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used primarily in organic synthesis, this compound serves as a key reagent for introducing the trifluoromethylphenylsulfonyl group into molecules. It is widely employed in the preparation of sulfonamides, which are valuable in pharmaceutical research for developing drugs with antibacterial, antiviral, or anticancer properties. Additionally, it is utilized in the production of agrochemicals, where the trifluoromethyl group enhances the biological activity of pesticides and herbicides. Its reactivity with amines and alcohols makes it a versatile building block in the synthesis of complex organic compounds.
Product Specification:
Test | Specification |
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PurityGC | 97.5 100% |
PURITYARGENTMETRIC TITRATION | 97.5 100% |
Appreance | White or Colorles to Yellow to Orange powder to lump to clear liquid |
NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿300.00 |
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5.000 | 10-20 days | ฿620.00 |
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25.000 | 10-20 days | ฿1,380.00 |
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100.000 | 10-20 days | ฿5,160.00 |
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4-(Trifluoromethyl)benzene-1-sulfonyl chloride
Used primarily in organic synthesis, this compound serves as a key reagent for introducing the trifluoromethylphenylsulfonyl group into molecules. It is widely employed in the preparation of sulfonamides, which are valuable in pharmaceutical research for developing drugs with antibacterial, antiviral, or anticancer properties. Additionally, it is utilized in the production of agrochemicals, where the trifluoromethyl group enhances the biological activity of pesticides and herbicides. Its reactivity with amines and alcohols makes it a versatile building block in the synthesis of complex organic compounds.
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