tert-Butyl 3-isocyano-3-tosylpropanoate

97%

Reagent Code: #132032
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CAS Number 107914-00-1

science Other reagents with same CAS 107914-00-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.38 g/mol
Formula C₁₅H₁₉NO₄S
badge Registry Numbers
MDL Number MFCD16620553
inventory_2 Storage & Handling
Storage -20°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing heterocyclic compounds. Its isocyano group participates in multicomponent reactions, such as Ugi and Passerini reactions, enabling the efficient construction of complex molecules. The tosyl group stabilizes adjacent carbanions, making it useful in alkylation and cyclization reactions. Commonly employed in medicinal chemistry for developing peptidomimetics and bioactive molecule scaffolds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,180.00
inventory 1g
10-20 days ฿10,500.00
inventory 5g
10-20 days ฿39,840.00
tert-Butyl 3-isocyano-3-tosylpropanoate
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Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing heterocyclic compounds. Its isocyano group participates in multicomponent reactions, such as Ugi and Passerini reactions, enabling the efficient construction of complex molecules. The tosyl group stabilizes adjacent carbanions, making it useful in alkylation and cyclization reactions. Commonly employed in medicinal chemistry for developing peptidomimetics and bioactive molecule scaffolds.

Used as a key intermediate in organic synthesis, particularly in the preparation of nitrogen-containing heterocyclic compounds. Its isocyano group participates in multicomponent reactions, such as Ugi and Passerini reactions, enabling the efficient construction of complex molecules. The tosyl group stabilizes adjacent carbanions, making it useful in alkylation and cyclization reactions. Commonly employed in medicinal chemistry for developing peptidomimetics and bioactive molecule scaffolds.

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