4-[2-HYDROXY-3-[(1-METHYLETHYL)AMINO]PROPOXY]BENZALDEHYDE

95%

Reagent Code: #198050
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CAS Number 29122-74-5

science Other reagents with same CAS 29122-74-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.30 g/mol
Formula C₁₃H₁₉NO₃
badge Registry Numbers
MDL Number MFCD16251410
thermostat Physical Properties
Boiling Point 402.5±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.105±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of beta-adrenergic blocking agents, particularly in the production of cardioselective beta-blockers. Its aldehyde and hydroxy-amino functionalities allow for further chemical modifications, making it valuable in pharmaceutical development for hypertension and angina treatments. Commonly employed in reductive amination reactions to introduce amine-containing side chains essential for biological activity. Also utilized in research settings to develop novel analogs with improved pharmacokinetic profiles.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿37,910.00

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4-[2-HYDROXY-3-[(1-METHYLETHYL)AMINO]PROPOXY]BENZALDEHYDE
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Used as an intermediate in the synthesis of beta-adrenergic blocking agents, particularly in the production of cardioselective beta-blockers. Its aldehyde and hydroxy-amino functionalities allow for further chemical modifications, making it valuable in pharmaceutical development for hypertension and angina treatments. Commonly employed in reductive amination reactions to introduce amine-containing side chains essential for biological activity. Also utilized in research settings to develop novel analogs w

Used as an intermediate in the synthesis of beta-adrenergic blocking agents, particularly in the production of cardioselective beta-blockers. Its aldehyde and hydroxy-amino functionalities allow for further chemical modifications, making it valuable in pharmaceutical development for hypertension and angina treatments. Commonly employed in reductive amination reactions to introduce amine-containing side chains essential for biological activity. Also utilized in research settings to develop novel analogs with improved pharmacokinetic profiles.

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