2,4-Difluoro-3-iodo-1,5-dimethoxybenzene

≥95%

Reagent Code: #179575
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CAS Number 1560796-27-1

science Other reagents with same CAS 1560796-27-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.04 g/mol
Formula C₈H₇F₂IO₂
badge Registry Numbers
MDL Number MFCD32706360
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its iodine and methoxy functional groups allow for selective cross-coupling reactions, making it valuable in building complex molecules. Commonly employed in medicinal chemistry for creating analogs with enhanced metabolic stability and bioavailability. Also utilized in research settings for labeling and tracer studies due to the presence of halogen atoms that facilitate detection and binding analysis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿45,000.00

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2,4-Difluoro-3-iodo-1,5-dimethoxybenzene
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its iodine and methoxy functional groups allow for selective cross-coupling reactions, making it valuable in building complex molecules. Commonly employed in medicinal chemistry for creating analogs with enhanced metabolic stability and bioavailability. Also utilized in research settings for labeling and tracer studies due to the presence of halogen atoms that f

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its iodine and methoxy functional groups allow for selective cross-coupling reactions, making it valuable in building complex molecules. Commonly employed in medicinal chemistry for creating analogs with enhanced metabolic stability and bioavailability. Also utilized in research settings for labeling and tracer studies due to the presence of halogen atoms that facilitate detection and binding analysis.

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