1,4-Difluoro-2-(methoxymethoxy)benzene

98%

Reagent Code: #180154
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CAS Number 749230-16-8

science Other reagents with same CAS 749230-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.14 g/mol
Formula C₈H₈F₂O₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds where the fluorine atoms enhance metabolic stability and bioavailability. The methoxymethoxy group acts as a protecting group for phenols during multi-step syntheses, allowing selective reactions at other sites on the molecule. Commonly employed in the preparation of active ingredients in crop protection agents and in the construction of complex drug molecules requiring aromatic ring modifications. Its stability and reactivity profile make it suitable for cross-coupling reactions and nucleophilic aromatic substitutions in controlled environments.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,040.00
inventory 250mg
10-20 days ฿1,750.00
inventory 1g
10-20 days ฿3,530.00
inventory 5g
10-20 days ฿10,600.00
inventory 25g
10-20 days ฿35,330.00

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1,4-Difluoro-2-(methoxymethoxy)benzene
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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 fluorine atoms enhance metabolic stability and bioavailability. The methoxymethoxy group acts as a protecting group for phenols during multi-step syntheses, allowing selective reactions at other sites on the molecule. Commonly employed in the preparation of active ingredients in crop protection agents and in the construction of complex drug molecules re

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds where the fluorine atoms enhance metabolic stability and bioavailability. The methoxymethoxy group acts as a protecting group for phenols during multi-step syntheses, allowing selective reactions at other sites on the molecule. Commonly employed in the preparation of active ingredients in crop protection agents and in the construction of complex drug molecules requiring aromatic ring modifications. Its stability and reactivity profile make it suitable for cross-coupling reactions and nucleophilic aromatic substitutions in controlled environments.

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