2-Methoxy-3-(trifluoromethyl)pyridine-5-boronic Acid Pinacol Ester

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Reagent Code: #89842
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CAS Number 1150561-61-7

science Other reagents with same CAS 1150561-61-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.09 g/mol
Formula C₁₃H₁₇F₃NO₃B
badge Registry Numbers
MDL Number MFCD12026094
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for introducing the 2-methoxy-3-(trifluoromethyl)pyridine moiety into more complex molecules. Its stability and reactivity make it valuable in pharmaceutical research, where it is used to develop novel drug candidates, especially those targeting neurological and inflammatory diseases. Additionally, it finds applications in agrochemical synthesis for creating compounds with enhanced biological activity. Its trifluoromethyl group contributes to improved metabolic stability and bioavailability in the final products.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿19,953.00
inventory 5g
10-20 days ฿61,137.00

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2-Methoxy-3-(trifluoromethyl)pyridine-5-boronic Acid Pinacol Ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for introducing the 2-methoxy-3-(trifluoromethyl)pyridine moiety into more complex molecules. Its stability and reactivity make it valuable in pharmaceutical research, where it is used to develop novel drug candidates, especially those targeting neurological and inflammatory diseases. Additionally, it finds applications in agrochem

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for introducing the 2-methoxy-3-(trifluoromethyl)pyridine moiety into more complex molecules. Its stability and reactivity make it valuable in pharmaceutical research, where it is used to develop novel drug candidates, especially those targeting neurological and inflammatory diseases. Additionally, it finds applications in agrochemical synthesis for creating compounds with enhanced biological activity. Its trifluoromethyl group contributes to improved metabolic stability and bioavailability in the final products.

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