1-Bromo-4-(1-(trifluoromethyl)cyclopropyl)benzene

95%

Reagent Code: #150020
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CAS Number 1227160-18-0

science Other reagents with same CAS 1227160-18-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.07 g/mol
Formula C₁₀H₈BrF₃
badge Registry Numbers
MDL Number MFCD16817615
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its bromoaryl group enables cross-coupling reactions, such as Suzuki or Heck reactions, allowing for the construction of complex organic molecules. The presence of the trifluoromethylcyclopropyl moiety contributes to increased lipophilicity and electron-withdrawing properties, making it valuable in the design of biologically active compounds, including potential candidates in medicinal chemistry for CNS agents or anti-inflammatory drugs. Also employed in materials science for creating specialty organic semiconductors or liquid crystals due to its rigid structure and electronic characteristics.

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Test Parameter Specification
Appearance Colorless to Light Yellow Liquid
Purity (%) 94.5-100%
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,600.00
inventory 250mg
10-20 days ฿2,400.00
inventory 500mg
10-20 days ฿3,600.00
inventory 1g
10-20 days ฿4,800.00
inventory 5g
10-20 days ฿16,000.00
inventory 10g
10-20 days ฿28,800.00
inventory 25g
10-20 days ฿57,600.00

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1-Bromo-4-(1-(trifluoromethyl)cyclopropyl)benzene
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its bromoaryl group enables cross-coupling reactions, such as Suzuki or Heck reactions, allowing for the construction of complex organic molecules. The presence of the trifluoromethylcyclopropyl moiety contributes to increased lipophilicity and electron-withdrawing properties, making it valuable in the design of b

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds with enhanced metabolic stability and bioavailability. Its bromoaryl group enables cross-coupling reactions, such as Suzuki or Heck reactions, allowing for the construction of complex organic molecules. The presence of the trifluoromethylcyclopropyl moiety contributes to increased lipophilicity and electron-withdrawing properties, making it valuable in the design of biologically active compounds, including potential candidates in medicinal chemistry for CNS agents or anti-inflammatory drugs. Also employed in materials science for creating specialty organic semiconductors or liquid crystals due to its rigid structure and electronic characteristics.

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