4-(2-Oxopyrrolidin-1-yl)benzaldehyde

95%

Reagent Code: #222091
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CAS Number 36151-45-8

science Other reagents with same CAS 36151-45-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.21 g/mol
Formula C₁₁H₁₁NO₂
badge Registry Numbers
MDL Number MFCD00454011
thermostat Physical Properties
Melting Point 121 °C
Boiling Point 454.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.243±0.06 g/cm3(Predicted)
Storage 2-8°C, inert atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs such as piracetam and related racetam family compounds. It plays a key role in constructing the core structure of these cognitive enhancers by enabling the formation of amide or ester linkages through its aldehyde functional group. Also utilized in organic synthesis for developing heterocyclic compounds and in medicinal chemistry for creating analogs with potential neuroprotective or stimulant properties. Its reactivity allows for easy modification, making it valuable in drug discovery and development.

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inventory 1g
10-20 days ฿25,690.00

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4-(2-Oxopyrrolidin-1-yl)benzaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs such as piracetam and related racetam family compounds. It plays a key role in constructing the core structure of these cognitive enhancers by enabling the formation of amide or ester linkages through its aldehyde functional group. Also utilized in organic synthesis for developing heterocyclic compounds and in medicinal chemistry for creating analogs with potential neuroprotective or stimulant prop
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of nootropic drugs such as piracetam and related racetam family compounds. It plays a key role in constructing the core structure of these cognitive enhancers by enabling the formation of amide or ester linkages through its aldehyde functional group. Also utilized in organic synthesis for developing heterocyclic compounds and in medicinal chemistry for creating analogs with potential neuroprotective or stimulant properties. Its reactivity allows for easy modification, making it valuable in drug discovery and development.
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