(R)-2-(1-Amino-2-hydroxyethyl)phenol

95%

Reagent Code: #228580
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CAS Number 1213028-30-8

science Other reagents with same CAS 1213028-30-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.17 g/mol
Formula C₈H₁₁NO₂
thermostat Physical Properties
Boiling Point 359.6±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.249±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of beta-blockers, which are medications designed to treat cardiovascular conditions such as hypertension, angina, and arrhythmias. Its chiral structure makes it valuable in creating enantiomerically pure drugs, improving therapeutic efficacy and reducing side effects. Also employed in research for developing new bioactive molecules and asymmetric synthesis due to its functional groups that allow for selective chemical modifications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,610.00
inventory 1g
10-20 days ฿39,390.00

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(R)-2-(1-Amino-2-hydroxyethyl)phenol
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Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of beta-blockers, which are medications designed to treat cardiovascular conditions such as hypertension, angina, and arrhythmias. Its chiral structure makes it valuable in creating enantiomerically pure drugs, improving therapeutic efficacy and reducing side effects. Also employed in research for developing new bioactive molecules and asymmetric synthesis due to its functional groups that allow for selective chem

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of beta-blockers, which are medications designed to treat cardiovascular conditions such as hypertension, angina, and arrhythmias. Its chiral structure makes it valuable in creating enantiomerically pure drugs, improving therapeutic efficacy and reducing side effects. Also employed in research for developing new bioactive molecules and asymmetric synthesis due to its functional groups that allow for selective chemical modifications.

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