Potassium trifluoro(4-(morpholine-4-carbonyl)phenyl)borate

95%

Reagent Code: #222612
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CAS Number 1314957-11-3

science Other reagents with same CAS 1314957-11-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.12 g/mol
Formula C₁₁H₁₂BF₃KNO₂
badge Registry Numbers
MDL Number MFCD09800742
thermostat Physical Properties
Melting Point 195-200 °C
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its borate structure provides enhanced stability and reactivity with aryl halides, making it valuable in constructing biaryl compounds found in active pharmaceutical ingredients. Particularly useful in late-stage functionalization due to its tolerance of various functional groups. Also employed in the development of novel drug candidates and in medicinal chemistry research for creating complex organic molecules with high selectivity and yield.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,210.00
inventory 1g
10-20 days ฿3,190.00
inventory 5g
10-20 days ฿11,120.00
Potassium trifluoro(4-(morpholine-4-carbonyl)phenyl)borate
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Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its borate structure provides enhanced stability and reactivity with aryl halides, making it valuable in constructing biaryl compounds found in active pharmaceutical ingredients. Particularly useful in late-stage functionalization due to its tolerance of various functional groups. Also employed in the development of novel drug candidates and in medicinal chemistry r

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical synthesis. Its borate structure provides enhanced stability and reactivity with aryl halides, making it valuable in constructing biaryl compounds found in active pharmaceutical ingredients. Particularly useful in late-stage functionalization due to its tolerance of various functional groups. Also employed in the development of novel drug candidates and in medicinal chemistry research for creating complex organic molecules with high selectivity and yield.

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