4-Nitrobenzenesulfonyl chloride
98%
- Product Code: 119535
Alias:
p-Nitrobenzenesulfonyl chloride
CAS:
98-74-8
Molecular Weight: | 221.62 g./mol | Molecular Formula: | C₆H₄ClNO₄S |
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EC Number: | 202-697-9 | MDL Number: | MFCD00007445 |
Melting Point: | 75 °C | Boiling Point: | 143-144 °C (1.5002 mmHg) |
Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
4-Nitrobenzenesulfonyl chloride is widely used in organic synthesis as a reagent for the preparation of sulfonamides, which are important in pharmaceutical and medicinal chemistry. It acts as a sulfonating agent, introducing the sulfonyl group into various organic compounds. This chemical is particularly valuable in peptide chemistry, where it is employed to protect amino groups during peptide synthesis. Additionally, it is utilized in the synthesis of dyes, agrochemicals, and other fine chemicals due to its ability to form stable sulfonamide derivatives. Its reactivity with amines makes it a key component in the development of biologically active molecules and intermediates in drug discovery.
Product Specification:
Test | Specification |
---|---|
Melting Point | 76-80 |
Purity (Hplc) | 98 |
Purity (Titration With Agno3) | 97.5-102.5 |
Appearance | Yellow To Brown Powder Or Crystals |
Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | ฿370.00 |
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25.000 | 10-20 days | ฿540.00 |
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100.000 | 10-20 days | ฿1,140.00 |
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500.000 | 10-20 days | ฿4,240.00 |
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2500.000 | 10-20 days | ฿18,160.00 |
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4-Nitrobenzenesulfonyl chloride
4-Nitrobenzenesulfonyl chloride is widely used in organic synthesis as a reagent for the preparation of sulfonamides, which are important in pharmaceutical and medicinal chemistry. It acts as a sulfonating agent, introducing the sulfonyl group into various organic compounds. This chemical is particularly valuable in peptide chemistry, where it is employed to protect amino groups during peptide synthesis. Additionally, it is utilized in the synthesis of dyes, agrochemicals, and other fine chemicals due to its ability to form stable sulfonamide derivatives. Its reactivity with amines makes it a key component in the development of biologically active molecules and intermediates in drug discovery.
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