2-(3-(trifluoromethoxy)phenyl)propan-2-amine hydrochloride

95%

Reagent Code: #241770
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CAS Number 1314665-58-1

science Other reagents with same CAS 1314665-58-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.06 g/mol
Formula C₁₀H₁₃ClF₃NO
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block in the production of selective adrenergic receptor modulators. Commonly applied in research settings for the preparation of bioactive molecules and analogs targeting neurological disorders. The trifluoromethoxy substituent enhances lipophilicity, aiding in cell membrane permeability and improving target specificity for potential reduced side effects. Also utilized in synthesis due to its amine functionality, enabling the construction of complex drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,574.00
inventory 250mg
10-20 days ฿6,480.00
inventory 500mg
10-20 days ฿12,150.00
inventory 50mg
10-20 days ฿1,584.00

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2-(3-(trifluoromethoxy)phenyl)propan-2-amine hydrochloride
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block in the production of selective adrenergic receptor modulators. Commonly applied in research settings for the preparation of bioactive molecules and analogs targeting neurological disorders. The trifluoromethoxy substituent enhances lipophilicity, aiding in cell membrane permeability and improving target specificity for potential reduced side effects.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents. It serves as a building block in the production of selective adrenergic receptor modulators. Commonly applied in research settings for the preparation of bioactive molecules and analogs targeting neurological disorders. The trifluoromethoxy substituent enhances lipophilicity, aiding in cell membrane permeability and improving target specificity for potential reduced side effects. Also utilized in synthesis due to its amine functionality, enabling the construction of complex drug candidates.

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