tert-Butyl (1,3-dioxo-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindol-2(3H)-yl) carbonate

≥98%

Reagent Code: #84736
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CAS Number 64205-15-8

science Other reagents with same CAS 64205-15-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.29 g/mol
Formula C₁₄H₁₇NO₅
thermostat Physical Properties
Boiling Point 360.898ºC
inventory_2 Storage & Handling
Density 1.33g/cm3
Storage room temperature, dry

description Product Description

This compound is a tert-butoxycarbonyl (Boc)-protected derivative of 3a,4,7,7a-tetrahydro-4,7-methano-1H-isoindole-1,3(2H)-dione, serving as a key intermediate in organic synthesis. It is particularly valuable in peptide chemistry and the development of pharmaceuticals or bioactive molecules, where the Boc group temporarily protects the imide nitrogen, enabling selective functionalization of the bicyclic scaffold. The protection facilitates complex transformations, and the Boc group can be readily deprotected under mild acidic conditions to reveal the free imide for further reactions.

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inventory 1g
10-20 days ฿880.00

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tert-Butyl (1,3-dioxo-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindol-2(3H)-yl) carbonate
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This compound is a tert-butoxycarbonyl (Boc)-protected derivative of 3a,4,7,7a-tetrahydro-4,7-methano-1H-isoindole-1,3(2H)-dione, serving as a key intermediate in organic synthesis. It is particularly valuable in peptide chemistry and the development of pharmaceuticals or bioactive molecules, where the Boc group temporarily protects the imide nitrogen, enabling selective functionalization of the bicyclic scaffold. The protection facilitates complex transformations, and the Boc group can be readily deprotect
This compound is a tert-butoxycarbonyl (Boc)-protected derivative of 3a,4,7,7a-tetrahydro-4,7-methano-1H-isoindole-1,3(2H)-dione, serving as a key intermediate in organic synthesis. It is particularly valuable in peptide chemistry and the development of pharmaceuticals or bioactive molecules, where the Boc group temporarily protects the imide nitrogen, enabling selective functionalization of the bicyclic scaffold. The protection facilitates complex transformations, and the Boc group can be readily deprotected under mild acidic conditions to reveal the free imide for further reactions.
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