1,3-Difluoro-4-iodo-2-methylbenzene

97%

Reagent Code: #178131
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CAS Number 1208077-89-7

science Other reagents with same CAS 1208077-89-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.02 g/mol
Formula C₇H₅F₂I
badge Registry Numbers
MDL Number MFCD12922605
inventory_2 Storage & Handling
Storage Room temperature, avoid light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds where the presence of fluorine enhances metabolic stability and bioavailability. The iodo group allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in building complex aromatic structures. Its methyl and fluoro substituents influence electronic and steric properties, useful in fine-tuning reactivity in medicinal chemistry and materials science applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿11,410.00
250mg
10-20 days ฿17,090.00
1g
10-20 days ฿42,690.00
1,3-Difluoro-4-iodo-2-methylbenzene
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds where the presence of fluorine enhances metabolic stability and bioavailability. The iodo group allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in building complex aromatic structures. Its methyl and fluoro substituents influence electronic and steric properties, useful in fine-tuning reactivi

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds where the presence of fluorine enhances metabolic stability and bioavailability. The iodo group allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, making it valuable in building complex aromatic structures. Its methyl and fluoro substituents influence electronic and steric properties, useful in fine-tuning reactivity in medicinal chemistry and materials science applications.

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