(S)-1-(4-(Trifluoromethoxy)phenyl)ethanamine hydrochloride

≥95%

Reagent Code: #235653
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CAS Number 1391540-47-8

science Other reagents with same CAS 1391540-47-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.64 g/mol
Formula C₉H₁₁ClF₃NO
badge Registry Numbers
MDL Number MFCD12757222
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules with high enantioselectivity, making it valuable in drug discovery for antidepressants, antipsychotics, and other neurologically active compounds. The amine functionality allows for easy derivatization, enabling rapid generation of compound libraries for screening. Its trifluoromethoxy aromatic group enhances metabolic stability and membrane permeability, beneficial traits in optimizing drug candidates.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,010.00
(S)-1-(4-(Trifluoromethoxy)phenyl)ethanamine hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules with high enantioselectivity, making it valuable in drug discovery for antidepressants, antipsychotics, and other neurologically active compounds. The amine functionality allows for easy derivatization, enabling rapid generation of compound libraries for screening. Its trifluoromethoxy aromatic group enhances meta

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. Its structure supports the creation of bioactive molecules with high enantioselectivity, making it valuable in drug discovery for antidepressants, antipsychotics, and other neurologically active compounds. The amine functionality allows for easy derivatization, enabling rapid generation of compound libraries for screening. Its trifluoromethoxy aromatic group enhances metabolic stability and membrane permeability, beneficial traits in optimizing drug candidates.

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