4-((benzyloxy)carbonyl)-2,6-difluorobenzoic acid

97%(HPLC) 

Reagent Code: #46041
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CAS Number 1403326-83-9

science Other reagents with same CAS 1403326-83-9

blur_circular Chemical Specifications

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Weight 292.23 g/mol
Formula C₁₅H₁₀F₂O₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in organic synthesis as a building block for more complex molecules, particularly in pharmaceutical research. Its structure, featuring both a benzyloxycarbonyl protecting group and difluoro substitution, makes it valuable for designing and synthesizing potential drug candidates. The difluoro groups can enhance the metabolic stability and bioavailability of the resulting compounds, while the benzyloxycarbonyl group can be selectively removed under mild conditions, allowing for further functionalization. It is often employed in the development of enzyme inhibitors, receptor modulators, and other bioactive molecules, particularly in medicinal chemistry projects targeting diseases where fluorine-containing compounds are advantageous.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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4-((benzyloxy)carbonyl)-2,6-difluorobenzoic acid
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This compound is primarily utilized in organic synthesis as a building block for more complex molecules, particularly in pharmaceutical research. Its structure, featuring both a benzyloxycarbonyl protecting group and difluoro substitution, makes it valuable for designing and synthesizing potential drug candidates. The difluoro groups can enhance the metabolic stability and bioavailability of the resulting compounds, while the benzyloxycarbonyl group can be selectively removed under mild conditions, allow

This compound is primarily utilized in organic synthesis as a building block for more complex molecules, particularly in pharmaceutical research. Its structure, featuring both a benzyloxycarbonyl protecting group and difluoro substitution, makes it valuable for designing and synthesizing potential drug candidates. The difluoro groups can enhance the metabolic stability and bioavailability of the resulting compounds, while the benzyloxycarbonyl group can be selectively removed under mild conditions, allowing for further functionalization. It is often employed in the development of enzyme inhibitors, receptor modulators, and other bioactive molecules, particularly in medicinal chemistry projects targeting diseases where fluorine-containing compounds are advantageous.

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