N-Allyl-p-toluenesulfonamide is a chemical compound widely used as a building block in organic synthesis. It plays a crucial role in laboratories where complex organic molecules are being developed. This compound is particularly valuable for its ability to participate in various chemical reactions, including substitution and bond formation processes. Its versatility makes it an essential tool for chemists working on the synthesis of heterocyclic compounds and bioactive molecules.
The compound’s chemical stability and high reactivity make it a preferred choice for synthetic chemists. Its molecular structure, featuring a toluenesulfonamide group, provides both stability and reactivity, enabling it to interact effectively with a wide range of reagents. This makes it suitable for nucleophilic and electrophilic reactions, which are common in organic chemistry. Its ability to form stable intermediates under different reaction conditions further enhances its utility in laboratory settings.
In Indonesian laboratories, N-Allyl-p-toluenesulfonamide is commonly used in research and development projects focused on organic chemistry. It is a key component in the synthesis of compounds with specific structural features, such as heterocycles and bioactive agents. Its reliability and performance in various reaction conditions make it a go-to material for both academic and industrial research in the region.
Related TCI products
- TCI T1461 4104-47-6 N-Sulfinyl-p-toluenesulfonamide
- TCI B3082 1576-37-0 N-Benzyl-p-toluenesulfonamide
- TCI B3051 33528-13-1 N-Benzyl-N-nitroso-p-toluenesulfonamide
- TCI B1389 2651-15-2 N-[Bis(methylthio)methylene]-p-toluenesulfonamide
- TCI B0745 1907-65-9 N-Butyl-p-toluenesulfonamide
- TCI T0285 649-15-0 N,N-Diethyl-p-toluenesulfonamide
- Organic synthesis of heterocyclic compounds due to its reactivity and structural versatility.
- Development of bioactive molecules as it can participate in nucleophilic and electrophilic reactions.
- Preparation of complex organic structures in academic and industrial research settings.
- Facilitation of substitution reactions through its stable toluenesulfonamide group.
- Use in molecular building blocks for creating new chemical entities with specific functional groups.
| Brand | TCI |
|---|---|
| CAS number | 50487-71-3 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Building Blocks > Non-Heterocyclic Building Blocks |
| Pack sizes | Available in various quantities as per standard laboratory supply |
| Physical form | Solid |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
N-Allyl-p-toluenesulfonamide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. The compound should be stored away from direct sunlight and heat sources to avoid degradation. Suitable containers for storage include airtight glass or plastic vessels. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment. Regular monitoring of storage conditions ensures the compound remains effective for its intended applications.
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