(S)-2-Amino-2-(3-(methoxymethyl)phenyl)ethanol hydrochloride

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Reagent Code: #113727
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CAS Number 2061996-45-8

science Other reagents with same CAS 2061996-45-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.69 g/mol
Formula C₁₂H₁₄N₂O₂
badge Registry Numbers
MDL Number MFCD30609575
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of drugs targeting neurological and cardiovascular disorders. The presence of both amino and hydroxyl groups allows for versatile chemical modifications, making it a key building block in creating molecules with specific biological activities. Additionally, it is employed in research settings to study receptor interactions and develop compounds with potential therapeutic effects. Its application extends to the production of chiral drugs, where its stereochemistry plays a crucial role in enhancing drug efficacy and reducing side effects.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,178.00
inventory 250mg
10-20 days ฿22,356.00

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(S)-2-Amino-2-(3-(methoxymethyl)phenyl)ethanol hydrochloride
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This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of drugs targeting neurological and cardiovascular disorders. The presence of both amino and hydroxyl groups allows for versatile chemical modifications, making it a key building block in creating molecules with specific biological activities. Additionally, it is employed in research settings t

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure is particularly valuable in the development of drugs targeting neurological and cardiovascular disorders. The presence of both amino and hydroxyl groups allows for versatile chemical modifications, making it a key building block in creating molecules with specific biological activities. Additionally, it is employed in research settings to study receptor interactions and develop compounds with potential therapeutic effects. Its application extends to the production of chiral drugs, where its stereochemistry plays a crucial role in enhancing drug efficacy and reducing side effects.

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