2-Phthalimidoacetaldehyde Diethyl Acetal

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Reagent Code: #225548
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CAS Number 78902-09-7

science Other reagents with same CAS 78902-09-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.29 g/mol
Formula C₁₄H₁₇NO₄
badge Registry Numbers
MDL Number MFCD00005901
thermostat Physical Properties
Melting Point 72°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of amino acids and heterocyclic compounds. Its aldehyde functionality, protected as a diethyl acetal, allows selective reactions in multi-step syntheses. It is also employed in the production of pharmaceuticals and agrochemicals where controlled release of the aldehyde group is required. The phthalimide moiety acts as a protecting group for amines, making this compound valuable in peptide synthesis and the construction of nitrogen-containing molecules.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿275.00
inventory 25g
10-20 days ฿852.50

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2-Phthalimidoacetaldehyde Diethyl Acetal
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Used as an intermediate in organic synthesis, particularly in the preparation of amino acids and heterocyclic compounds. Its aldehyde functionality, protected as a diethyl acetal, allows selective reactions in multi-step syntheses. It is also employed in the production of pharmaceuticals and agrochemicals where controlled release of the aldehyde group is required. The phthalimide moiety acts as a protecting group for amines, making this compound valuable in peptide synthesis and the construction of nitro

Used as an intermediate in organic synthesis, particularly in the preparation of amino acids and heterocyclic compounds. Its aldehyde functionality, protected as a diethyl acetal, allows selective reactions in multi-step syntheses. It is also employed in the production of pharmaceuticals and agrochemicals where controlled release of the aldehyde group is required. The phthalimide moiety acts as a protecting group for amines, making this compound valuable in peptide synthesis and the construction of nitrogen-containing molecules.

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