N-(6-Aminohexyl)-2-nitrobenzenesulfonamide Hydrochloride
≥95%
- Product Code: 121401
CAS:
95915-82-5
| Molecular Weight: | 337.82 g./mol | Molecular Formula: | C₁₂H₁₉N₃O₄SHCl |
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| EC Number: | MDL Number: | MFCD06797045 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily used in organic synthesis as a protecting group for amines during complex chemical reactions. Its structure allows it to temporarily shield amine functionalities, preventing unwanted side reactions while other parts of the molecule are modified. This is particularly useful in peptide synthesis, where selective protection and deprotection of amino groups are critical. Additionally, it can serve as a reagent in biochemical research, aiding in the study of enzyme interactions or protein modifications. Its water solubility, due to the hydrochloride form, makes it convenient for use in aqueous solutions, expanding its applicability in various laboratory settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿1,314.00 |
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| 1.000 | 10-20 days | ฿3,591.00 |
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N-(6-Aminohexyl)-2-nitrobenzenesulfonamide Hydrochloride
This compound is primarily used in organic synthesis as a protecting group for amines during complex chemical reactions. Its structure allows it to temporarily shield amine functionalities, preventing unwanted side reactions while other parts of the molecule are modified. This is particularly useful in peptide synthesis, where selective protection and deprotection of amino groups are critical. Additionally, it can serve as a reagent in biochemical research, aiding in the study of enzyme interactions or protein modifications. Its water solubility, due to the hydrochloride form, makes it convenient for use in aqueous solutions, expanding its applicability in various laboratory settings.
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