1-(Difluoromethoxy)-3-Iodobenzene

97%

Reagent Code: #179128
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CAS Number 518070-17-2

science Other reagents with same CAS 518070-17-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.02 g/mol
Formula C₇H₅F₂IO
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the difluoromethoxy group enhances metabolic stability and membrane permeability. Its iodine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. Commonly employed in medicinal chemistry for optimizing lead compounds in CNS-targeted drugs and oncology research due to improved lipophilicity and bioavailability profiles. Also utilized in agrochemical research for designing novel active ingredients with enhanced environmental stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿490.00
250mg
10-20 days ฿1,100.00
1g
10-20 days ฿2,130.00
5g
10-20 days ฿3,260.00
1-(Difluoromethoxy)-3-Iodobenzene
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the difluoromethoxy group enhances metabolic stability and membrane permeability. Its iodine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. Commonly employed in medicinal chemistry for optimizing lead compounds in CNS-targeted drugs and oncology research

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the difluoromethoxy group enhances metabolic stability and membrane permeability. Its iodine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. Commonly employed in medicinal chemistry for optimizing lead compounds in CNS-targeted drugs and oncology research due to improved lipophilicity and bioavailability profiles. Also utilized in agrochemical research for designing novel active ingredients with enhanced environmental stability.

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