4-(trifluoromethyl)thiazol-2-amine

95%

Reagent Code: #240267
label
Alias 2-amino-4-trifluoromethyl-1,3-thiazole; 4-trifluoromethyl-thiazole-2-amine; 4-(TRIFLUOROMETHYL)-1,3-THIAZOL-2-AMINE
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CAS Number 349-49-5

science Other reagents with same CAS 349-49-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.14 g/mol
Formula C₄H₃F₃N₂S
badge Registry Numbers
MDL Number MFCD00832759
thermostat Physical Properties
Melting Point 60-62℃
Boiling Point 214℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.557±0.06 g/ml(Predicted)
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the design of kinase inhibitors and bioactive molecules due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability and membrane permeability. Also employed in agrochemicals for creating herbicides and pesticides, where the thiazole ring contributes to improved biological activity and selectivity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿286.00
inventory 5g
10-20 days ฿2,340.00
4-(trifluoromethyl)thiazol-2-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the design of kinase inhibitors and bioactive molecules due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability and membrane permeability. Also employed in agrochemicals for creating herbicides and pesticides, where the thiazole ring contributes to improved biological activity and selectivity. Commonly utilized in medicinal

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure supports the design of kinase inhibitors and bioactive molecules due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability and membrane permeability. Also employed in agrochemicals for creating herbicides and pesticides, where the thiazole ring contributes to improved biological activity and selectivity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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