potassium trifluoro(2-hydroxyphenyl)borate(1-)

98%

Reagent Code: #226138
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CAS Number 850313-92-7

science Other reagents with same CAS 850313-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.0078 g/mol
Formula C₆H₅BF₃KO
badge Registry Numbers
MDL Number MFCD07781243
thermostat Physical Properties
Melting Point >250℃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a reagent in organic synthesis, particularly in cross-coupling reactions involving phenolic compounds. It enables the formation of carbon-carbon bonds under mild conditions, making it valuable in pharmaceutical and agrochemical industries for constructing biaryl structures. Its stability and selectivity enhance reaction efficiency, especially in transformations where traditional boronic acids may decompose or require harsher conditions. Also employed in labeling and bioconjugation due to its compatibility with functional groups present in complex molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿840.00
inventory 5g
10-20 days ฿2,920.00
potassium trifluoro(2-hydroxyphenyl)borate(1-)
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Used as a reagent in organic synthesis, particularly in cross-coupling reactions involving phenolic compounds. It enables the formation of carbon-carbon bonds under mild conditions, making it valuable in pharmaceutical and agrochemical industries for constructing biaryl structures. Its stability and selectivity enhance reaction efficiency, especially in transformations where traditional boronic acids may decompose or require harsher conditions. Also employed in labeling and bioconjugation due to its comp

Used as a reagent in organic synthesis, particularly in cross-coupling reactions involving phenolic compounds. It enables the formation of carbon-carbon bonds under mild conditions, making it valuable in pharmaceutical and agrochemical industries for constructing biaryl structures. Its stability and selectivity enhance reaction efficiency, especially in transformations where traditional boronic acids may decompose or require harsher conditions. Also employed in labeling and bioconjugation due to its compatibility with functional groups present in complex molecules.

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