1-bromo-2-(2,2-difluorocyclopropyl)benzene

95%

Reagent Code: #148915
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CAS Number 1897571-62-8

science Other reagents with same CAS 1897571-62-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.97 g/mol
Formula C₉H₇BrF₂
badge Registry Numbers
MDL Number MFCD30002715
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules where the difluorocyclopropyl group enhances metabolic stability and lipophilicity. Its bromo functionality allows for further cross-coupling reactions, such as Suzuki or Negishi couplings, enabling the construction of complex aromatic systems in drug discovery. Also employed in the preparation of novel fluorinated building blocks for materials science and medicinal chemistry research.

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Test Parameter Specification
Appearance Colorless oily liquid
Purity (%) 95-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,130.00
inventory 1g
10-20 days ฿22,160.00
inventory 100mg
10-20 days ฿4,170.00

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1-bromo-2-(2,2-difluorocyclopropyl)benzene
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules where the difluorocyclopropyl group enhances metabolic stability and lipophilicity. Its bromo functionality allows for further cross-coupling reactions, such as Suzuki or Negishi couplings, enabling the construction of complex aromatic systems in drug discovery. Also employed in the preparation of novel fluorinated building blocks for materials science and m

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules where the difluorocyclopropyl group enhances metabolic stability and lipophilicity. Its bromo functionality allows for further cross-coupling reactions, such as Suzuki or Negishi couplings, enabling the construction of complex aromatic systems in drug discovery. Also employed in the preparation of novel fluorinated building blocks for materials science and medicinal chemistry research.

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