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2-Nitrobenzenesulfonyl chloride, 97%, Thermo Scientific Chemicals
Catalog number: B21522.14
25 g, Each
Thermo Scientific Chemicals
2-Nitrobenzenesulfonyl chloride, 97%, Thermo Scientific Chemicals
Catalog number: B21522.14
25 g, Each
Quantity
Catalog number: B21522.14
also known as B21522-14
Price (USD)
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42.65 50.10 Save 7.45 (14%)
Ends: 15-Oct-2024
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Chemical Identifiers
CAS
1694-92-4
IUPAC Name
2-nitrobenzene-1-sulfonyl chloride
Molecular Formula
C6H4ClNO4S
InChI Key
WPHUUIODWRNJLO-UHFFFAOYSA-N
SMILES
[O-][N+](=O)C1=CC=CC=C1S(Cl)(=O)=O
Specifications
Specification SheetAppearance (Color)
White to cream to brown
Form
Crystals or powder or crystalline powder or fused solid
Assay (Titration ex Chloride)
≥96.0 to ≤104.0%
Identification (FTIR)
Conforms
Melting Point (clear melt)
63.0-72.0?C
Description
2-Nitrobenzenesulfonyl chloride acts as a reagent to form 2-nitrobenzenesulfonyl derivatives of alcohols and amines. It is also involved in the selective cleavage with thiophenol without displacement of the nitro group. Further, it is used in the preparation of renin inhibitors. In addition to this, it finds application as an anticonvulsant.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Nitrobenzenesulfonyl chloride acts as a reagent to form 2-nitrobenzenesulfonyl derivatives of alcohols and amines. It is also involved in the selective cleavage with thiophenol without displacement of the nitro group. Further, it is used in the preparation of renin inhibitors. In addition to this, it finds application as an anticonvulsant.
Solubility
Soluble in toluene, tetrahydrofuran, methylene chloride, ethyl acetate and dimethylformamide. Insoluble in water.
Notes
Moisture sensitive. Incompatible with strong oxidizing agents and strong bases.
2-Nitrobenzenesulfonyl chloride acts as a reagent to form 2-nitrobenzenesulfonyl derivatives of alcohols and amines. It is also involved in the selective cleavage with thiophenol without displacement of the nitro group. Further, it is used in the preparation of renin inhibitors. In addition to this, it finds application as an anticonvulsant.
Solubility
Soluble in toluene, tetrahydrofuran, methylene chloride, ethyl acetate and dimethylformamide. Insoluble in water.
Notes
Moisture sensitive. Incompatible with strong oxidizing agents and strong bases.
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