5-(Trifluoromethyl)thiazol-2-amine

≥95%

Reagent Code: #241554
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CAS Number 169260-97-3

science Other reagents with same CAS 169260-97-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.14 g/mol
Formula C₄H₃F₃N₂S
badge Registry Numbers
MDL Number MFCD11846867
thermostat Physical Properties
Boiling Point 214℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.557±0.06g/ml(Predicted)
Storage 2-8℃, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal, antibacterial, and anticancer agents. Its structure supports the design of bioactive molecules due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability and membrane permeability. Commonly employed in agrochemicals for creating herbicides and pesticides, thanks to its ability to improve compound durability and target specificity. Also utilized in research settings for building novel heterocyclic compounds in drug discovery programs.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿960.00
inventory 250mg
10-20 days ฿1,970.00
inventory 1g
10-20 days ฿6,120.00
5-(Trifluoromethyl)thiazol-2-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal, antibacterial, and anticancer agents. Its structure supports the design of bioactive molecules due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability and membrane permeability. Commonly employed in agrochemicals for creating herbicides and pesticides, thanks to its ability to improve compound durability and target specificity. Also utilized in research settings for b

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal, antibacterial, and anticancer agents. Its structure supports the design of bioactive molecules due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability and membrane permeability. Commonly employed in agrochemicals for creating herbicides and pesticides, thanks to its ability to improve compound durability and target specificity. Also utilized in research settings for building novel heterocyclic compounds in drug discovery programs.

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