tert-Butyl tetrahydro-2H-pyrrolo[3,4-d]isothiazole-5(3H)-carboxylate 1,1-dioxide

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Reagent Code: #122366
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CAS Number 1823230-79-0

science Other reagents with same CAS 1823230-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.32 g/mol
Formula C₁₀H₁₈N₂O₄S
badge Registry Numbers
MDL Number MFCD26405881
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description 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.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿46,800.00
inventory 100mg
10-20 days ฿25,074.00

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tert-Butyl tetrahydro-2H-pyrrolo[3,4-d]isothiazole-5(3H)-carboxylate 1,1-dioxide
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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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