Benzamide, 5-(2-amino-1-hydroxyethyl)-2-hydroxy-

≥95%

Reagent Code: #141703
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CAS Number 68807-83-0

science Other reagents with same CAS 68807-83-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.2032 g/mol
Formula C₉H₁₂N₂O₃
badge Registry Numbers
MDL Number MFCD20693583
thermostat Physical Properties
Boiling Point 448.5±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.388±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of adrenergic receptor agonists and bronchodilators. Its structure supports the creation of compounds that target respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). The hydroxy and amino functional groups enable salt formation and enhance solubility, improving bioavailability in final drug products. Also employed in research settings for structure-activity relationship (SAR) studies of biologically active molecules.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿48,000.00
inventory 25mg
10-20 days ฿96,000.00
inventory 50mg
10-20 days ฿144,000.00

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Benzamide, 5-(2-amino-1-hydroxyethyl)-2-hydroxy-
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of adrenergic receptor agonists and bronchodilators. Its structure supports the creation of compounds that target respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). The hydroxy and amino functional groups enable salt formation and enhance solubility, improving bioavailability in final drug products. Also employed in research settings for structure-activity relationship (SAR) studies

Used in the synthesis of pharmaceutical intermediates, particularly in the development of adrenergic receptor agonists and bronchodilators. Its structure supports the creation of compounds that target respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). The hydroxy and amino functional groups enable salt formation and enhance solubility, improving bioavailability in final drug products. Also employed in research settings for structure-activity relationship (SAR) studies of biologically active molecules.

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