(S)-1-(4-Chloro-2-methylphenyl)ethanamine

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Reagent Code: #37923
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CAS Number 1213908-11-2

science Other reagents with same CAS 1213908-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.65 g/mol
Formula C₉H₁₂ClN
badge Registry Numbers
MDL Number MFCD08057551
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its chiral structure makes it valuable in the production of enantiomerically pure compounds, which are essential for drugs targeting specific biological pathways with minimal side effects. It is often employed in the creation of antihistamines, anti-inflammatory agents, and other medications that require precise stereochemistry for optimal efficacy. Additionally, it serves as a building block in organic synthesis for research and development of novel compounds with potential pharmacological activities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,205.00

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(S)-1-(4-Chloro-2-methylphenyl)ethanamine
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its chiral structure makes it valuable in the production of enantiomerically pure compounds, which are essential for drugs targeting specific biological pathways with minimal side effects. It is often employed in the creation of antihistamines, anti-inflammatory agents, and other medications that require precise stereochem

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its chiral structure makes it valuable in the production of enantiomerically pure compounds, which are essential for drugs targeting specific biological pathways with minimal side effects. It is often employed in the creation of antihistamines, anti-inflammatory agents, and other medications that require precise stereochemistry for optimal efficacy. Additionally, it serves as a building block in organic synthesis for research and development of novel compounds with potential pharmacological activities.

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