1-Bromo-2-cyclopropyl-4-fluoro-5-methoxybenzene

95%

Reagent Code: #130233
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CAS Number 1784088-25-0

science Other reagents with same CAS 1784088-25-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.09 g/mol
Formula C₁₀H₁₀BrFO
thermostat Physical Properties
Boiling Point 253.0±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.514±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure allows for selective functionalization, making it valuable in building complex aromatic frameworks in medicinal chemistry. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce the cyclopropyl-fluoro-methoxyaryl moiety into larger molecules. Also utilized in agrochemical research for designing novel active ingredients with improved metabolic stability and binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,740.00
inventory 250mg
10-20 days ฿23,480.00
inventory 50mg
10-20 days ฿6,910.00

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1-Bromo-2-cyclopropyl-4-fluoro-5-methoxybenzene
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure allows for selective functionalization, making it valuable in building complex aromatic frameworks in medicinal chemistry. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce the cyclopropyl-fluoro-methoxyaryl moiety into larger molecules. Also utilized in agrochemical re

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates targeting central nervous system disorders. Its structure allows for selective functionalization, making it valuable in building complex aromatic frameworks in medicinal chemistry. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to introduce the cyclopropyl-fluoro-methoxyaryl moiety into larger molecules. Also utilized in agrochemical research for designing novel active ingredients with improved metabolic stability and binding affinity.

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