(S)-5-(Benzyloxy)-2-(1,3-dioxoisoindolin-2-yl)-5-oxopentanoic acid

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Reagent Code: #235616
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CAS Number 88784-33-2

science Other reagents with same CAS 88784-33-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 367.35 g/mol
Formula C₂₀H₁₇NO₆
badge Registry Numbers
MDL Number MFCD13152207
thermostat Physical Properties
Melting Point 135-136°C
Boiling Point 588.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral center and functional groups make it valuable in asymmetric synthesis, where it helps introduce specific stereochemistry into target molecules. Commonly employed in the preparation of protease inhibitors and other therapeutic agents requiring precise three-dimensional structure. The phthalimide group acts as a protecting group and can be removed selectively, allowing further functionalization. Also utilized in peptide mimetics and drug discovery research due to its structural versatility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿670.00
inventory 250mg
10-20 days ฿1,550.00
inventory 1g
10-20 days ฿4,740.00
inventory 5g
10-20 days ฿20,550.00

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(S)-5-(Benzyloxy)-2-(1,3-dioxoisoindolin-2-yl)-5-oxopentanoic acid
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral center and functional groups make it valuable in asymmetric synthesis, where it helps introduce specific stereochemistry into target molecules. Commonly employed in the preparation of protease inhibitors and other therapeutic agents requiring precise three-dimensional structure. The phthalimide group acts as a protecting group and can be removed selectively, allowing f

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals. Its chiral center and functional groups make it valuable in asymmetric synthesis, where it helps introduce specific stereochemistry into target molecules. Commonly employed in the preparation of protease inhibitors and other therapeutic agents requiring precise three-dimensional structure. The phthalimide group acts as a protecting group and can be removed selectively, allowing further functionalization. Also utilized in peptide mimetics and drug discovery research due to its structural versatility.

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