alpha-Tosyl-(2-bromobenzyl)isocyanide
97%
- Product Code: 121758
CAS:
936548-16-2
| Molecular Weight: | 350.24 g./mol | Molecular Formula: | C₁₅H₁₂BrNO₂S |
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| EC Number: | MDL Number: | MFCD04114784 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecular frameworks. It serves as a versatile building block in multicomponent reactions, such as the Ugi reaction, where it aids in the formation of peptide-like structures and heterocyclic compounds. Its isocyanide group is highly reactive, enabling it to participate in cyclization and coupling reactions, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, the tosyl and bromobenzyl groups provide sites for further functionalization, making it valuable in the synthesis of bioactive molecules and advanced materials. Its application is particularly significant in medicinal chemistry for creating drug candidates with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,724.00 |
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| 1.000 | 10-20 days | ฿12,915.00 |
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alpha-Tosyl-(2-bromobenzyl)isocyanide
This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecular frameworks. It serves as a versatile building block in multicomponent reactions, such as the Ugi reaction, where it aids in the formation of peptide-like structures and heterocyclic compounds. Its isocyanide group is highly reactive, enabling it to participate in cyclization and coupling reactions, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, the tosyl and bromobenzyl groups provide sites for further functionalization, making it valuable in the synthesis of bioactive molecules and advanced materials. Its application is particularly significant in medicinal chemistry for creating drug candidates with improved efficacy and selectivity.
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