2,4-Dibromo-5-(trifluoromethyl)-1H-imidazole

95%

Reagent Code: #177465
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CAS Number 81654-02-6

science Other reagents with same CAS 81654-02-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.87 g/mol
Formula C₄HBr₂F₃N₂
badge Registry Numbers
MDL Number MFCD08458161
thermostat Physical Properties
Melting Point 166-168 °C
Boiling Point 313.4±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.316±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antifungal and antimicrobial agents. Its structure supports the development of bioactive molecules due to the presence of halogen and trifluoromethyl groups, which enhance metabolic stability and binding affinity. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profile. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies involving heterocyclic compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,170.00
inventory 250mg
10-20 days ฿12,100.00
inventory 1g
10-20 days ฿23,720.00

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2,4-Dibromo-5-(trifluoromethyl)-1H-imidazole
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antifungal and antimicrobial agents. Its structure supports the development of bioactive molecules due to the presence of halogen and trifluoromethyl groups, which enhance metabolic stability and binding affinity. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profile. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies invo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antifungal and antimicrobial agents. Its structure supports the development of bioactive molecules due to the presence of halogen and trifluoromethyl groups, which enhance metabolic stability and binding affinity. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profile. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies involving heterocyclic compounds.

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