N-(5-Bromothiazol-4-yl)-2,2,2-trifluoroacetamide

95%

Reagent Code: #218425
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CAS Number 1211593-45-1

science Other reagents with same CAS 1211593-45-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.05 g/mol
Formula C₅H₂BrF₃N₂OS
badge Registry Numbers
MDL Number MFCD11520318
inventory_2 Storage & Handling
Density 1.996±0.06 g/cm3 (20 ºC 760 Torr)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in agrochemicals and pharmaceuticals. Its structure supports the development of novel fungicides and insecticides due to the presence of bromine and trifluoroacetamide moieties, which enhance reactivity and binding properties. Also employed in medicinal chemistry research for designing kinase inhibitors and antimicrobial agents. The compound’s stability and functional groups make it suitable for cross-coupling reactions in heterocyclic chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,880.00
inventory 250mg
10-20 days ฿5,020.00
inventory 1g
10-20 days ฿15,200.00
N-(5-Bromothiazol-4-yl)-2,2,2-trifluoroacetamide
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Used as an intermediate in the synthesis of biologically active compounds, particularly in agrochemicals and pharmaceuticals. Its structure supports the development of novel fungicides and insecticides due to the presence of bromine and trifluoroacetamide moieties, which enhance reactivity and binding properties. Also employed in medicinal chemistry research for designing kinase inhibitors and antimicrobial agents. The compound’s stability and functional groups make it suitable for cross-coupling reactio

Used as an intermediate in the synthesis of biologically active compounds, particularly in agrochemicals and pharmaceuticals. Its structure supports the development of novel fungicides and insecticides due to the presence of bromine and trifluoroacetamide moieties, which enhance reactivity and binding properties. Also employed in medicinal chemistry research for designing kinase inhibitors and antimicrobial agents. The compound’s stability and functional groups make it suitable for cross-coupling reactions in heterocyclic chemistry.

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