(R)-3-(1-Aminopropyl)-5-(trifluoromethyl)phenol hydrochloride

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Reagent Code: #229156
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CAS Number 2411590-98-0

science Other reagents with same CAS 2411590-98-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.66 g/mol
Formula C₁₀H₁₃ClF₃NO
badge Registry Numbers
MDL Number MFCD32067825
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents. Its chiral amine structure makes it valuable in creating enantioselective drugs, especially those targeting neurological disorders. Commonly employed in research settings for optimizing drug candidates with improved selectivity and reduced side effects. Also utilized in the preparation of beta-adrenergic receptor modulators due to its structural similarity to known bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿34,260.00
inventory 250mg
10-20 days ฿51,390.00
inventory 1g
10-20 days ฿128,260.00

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(R)-3-(1-Aminopropyl)-5-(trifluoromethyl)phenol hydrochloride
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents. Its chiral amine structure makes it valuable in creating enantioselective drugs, especially those targeting neurological disorders. Commonly employed in research settings for optimizing drug candidates with improved selectivity and reduced side effects. Also utilized in the preparation of beta-adrenergic receptor modulators due to its structural similarity to known bioactive molecules.

Used in the synthesis of pharmaceutical intermediates, particularly in the development of central nervous system agents. Its chiral amine structure makes it valuable in creating enantioselective drugs, especially those targeting neurological disorders. Commonly employed in research settings for optimizing drug candidates with improved selectivity and reduced side effects. Also utilized in the preparation of beta-adrenergic receptor modulators due to its structural similarity to known bioactive molecules.

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