(S)-2-Amino-2-(3-methoxyphenyl)ethanol

97%

Reagent Code: #113724
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CAS Number 1213016-49-9

science Other reagents with same CAS 1213016-49-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.21 g/mol
Formula C₉H₁₃NO₂
badge Registry Numbers
MDL Number MFCD09253686
thermostat Physical Properties
Boiling Point 325.4±32.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Its chiral structure makes it valuable for creating enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it serves as a key intermediate in organic synthesis, contributing to the production of various bioactive molecules and fine chemicals. Its methoxy group enhances its reactivity and selectivity in chemical reactions, making it a versatile building block in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,585.00
inventory 1g
10-20 days ฿19,170.00

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(S)-2-Amino-2-(3-methoxyphenyl)ethanol
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This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Its chiral structure makes it valuable for creating enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it serves as a key intermediate in organic synthesis, contributing to the production of various bioactive molecules and fine chemicals. Its me

This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of beta-blockers, which are medications used to manage cardiovascular conditions like hypertension and arrhythmias. Its chiral structure makes it valuable for creating enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it serves as a key intermediate in organic synthesis, contributing to the production of various bioactive molecules and fine chemicals. Its methoxy group enhances its reactivity and selectivity in chemical reactions, making it a versatile building block in medicinal chemistry.

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