tert-Butyl tetrahydro-2H-pyrrolo[3,4-d]isothiazole-5(3H)-carboxylate 1,1-dioxide
97%
- Product Code: 122366
CAS:
1823230-79-0
| Molecular Weight: | 262.32 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₄S |
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| EC Number: | MDL Number: | MFCD26405881 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure is particularly valuable in the development of pharmaceuticals, especially in the synthesis of compounds with potential therapeutic properties. The tert-butyl group provides steric protection, enhancing the stability of the molecule during reactions, while the isothiazole moiety can contribute to biological activity. Researchers often employ this chemical in the construction of heterocyclic frameworks, which are common in drug discovery. Additionally, its unique structure makes it a candidate for exploring novel chemical transformations and catalytic processes in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿25,074.00 |
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| 0.250 | 10-20 days | ฿46,800.00 |
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tert-Butyl tetrahydro-2H-pyrrolo[3,4-d]isothiazole-5(3H)-carboxylate 1,1-dioxide
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure is particularly valuable in the development of pharmaceuticals, especially in the synthesis of compounds with potential therapeutic properties. The tert-butyl group provides steric protection, enhancing the stability of the molecule during reactions, while the isothiazole moiety can contribute to biological activity. Researchers often employ this chemical in the construction of heterocyclic frameworks, which are common in drug discovery. Additionally, its unique structure makes it a candidate for exploring novel chemical transformations and catalytic processes in medicinal chemistry.
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