tert-Butyl 3-oxopropanoate

95%

Reagent Code: #154577
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CAS Number 108350-21-6

science Other reagents with same CAS 108350-21-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 144.17 g/mol
Formula C₇H₁₂O₃
badge Registry Numbers
MDL Number MFCD22200887
inventory_2 Storage & Handling
Storage -20°C, Sealed, Drying, Inert Gas

description Product Description

Used primarily as a building block in organic synthesis, this compound serves as a key intermediate in the preparation of heterocyclic compounds, particularly pyrazoles and isoxazoles, which are common scaffolds in pharmaceuticals and agrochemicals. Its β-keto ester functionality allows for facile alkylation, condensation, and cyclization reactions. It is also employed in the synthesis of active pharmaceutical ingredients (APIs) where the tert-butyl ester group acts as a protecting group, enabling selective reactions at other functional sites. Additionally, it finds use in the development of specialty polymers and in the manufacture of flavor and fragrance compounds due to its reactivity in forming complex esters.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿21,550.00

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tert-Butyl 3-oxopropanoate
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Used primarily as a building block in organic synthesis, this compound serves as a key intermediate in the preparation of heterocyclic compounds, particularly pyrazoles and isoxazoles, which are common scaffolds in pharmaceuticals and agrochemicals. Its β-keto ester functionality allows for facile alkylation, condensation, and cyclization reactions. It is also employed in the synthesis of active pharmaceutical ingredients (APIs) where the tert-butyl ester group acts as a protecting group, enabling select

Used primarily as a building block in organic synthesis, this compound serves as a key intermediate in the preparation of heterocyclic compounds, particularly pyrazoles and isoxazoles, which are common scaffolds in pharmaceuticals and agrochemicals. Its β-keto ester functionality allows for facile alkylation, condensation, and cyclization reactions. It is also employed in the synthesis of active pharmaceutical ingredients (APIs) where the tert-butyl ester group acts as a protecting group, enabling selective reactions at other functional sites. Additionally, it finds use in the development of specialty polymers and in the manufacture of flavor and fragrance compounds due to its reactivity in forming complex esters.

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