1,3-Dioxoisoindolin-2-yl 3-methylbutanoate

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Reagent Code: #131125
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CAS Number 2125731-81-7

science Other reagents with same CAS 2125731-81-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.25 g/mol
Formula C₁₃H₁₃NO₄
thermostat Physical Properties
Boiling Point 370.8±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.29±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

1,3-Dioxoisoindolin-2-yl 3-methylbutanoate is an O-acyl derivative of N-hydroxyphthalimide, serving as an active ester in organic synthesis. It is primarily used for amide bond formation by reacting with amines to produce amides, releasing N-hydroxyphthalimide as a byproduct. This makes it valuable in peptide synthesis, pharmaceutical intermediate preparation, and fine chemical manufacturing, where mild reaction conditions and high efficiency are required. The compound exhibits good stability and solubility in common organic solvents, facilitating its use in various synthetic protocols.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,320.00
inventory 5g
10-20 days ฿12,590.00

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1,3-Dioxoisoindolin-2-yl 3-methylbutanoate
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1,3-Dioxoisoindolin-2-yl 3-methylbutanoate is an O-acyl derivative of N-hydroxyphthalimide, serving as an active ester in organic synthesis. It is primarily used for amide bond formation by reacting with amines to produce amides, releasing N-hydroxyphthalimide as a byproduct. This makes it valuable in peptide synthesis, pharmaceutical intermediate preparation, and fine chemical manufacturing, where mild reaction conditions and high efficiency are required. The compound exhibits good stability and solubil

1,3-Dioxoisoindolin-2-yl 3-methylbutanoate is an O-acyl derivative of N-hydroxyphthalimide, serving as an active ester in organic synthesis. It is primarily used for amide bond formation by reacting with amines to produce amides, releasing N-hydroxyphthalimide as a byproduct. This makes it valuable in peptide synthesis, pharmaceutical intermediate preparation, and fine chemical manufacturing, where mild reaction conditions and high efficiency are required. The compound exhibits good stability and solubility in common organic solvents, facilitating its use in various synthetic protocols.

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