(3-Morpholino-5-(trifluoromethyl) phenyl)boronic acid

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Reagent Code: #90124
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CAS Number 1704069-70-4

science Other reagents with same CAS 1704069-70-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.04 g/mol
Formula C₁₁H₁₃BF₃NO₃
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its trifluoromethyl group enhances the stability and reactivity of the resulting products, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for creating advanced polymers and coatings with specific properties. Its boronic acid moiety also allows for applications in sensor development, particularly in detecting sugars and other biologically relevant molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿44,770.00
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(3-Morpholino-5-(trifluoromethyl) phenyl)boronic acid
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its trifluoromethyl group enhances the stability and reactivity of the resulting products, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for creating advanced polymers and coatings with specific properties. Its boronic acid moiety also allows for

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its trifluoromethyl group enhances the stability and reactivity of the resulting products, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for creating advanced polymers and coatings with specific properties. Its boronic acid moiety also allows for applications in sensor development, particularly in detecting sugars and other biologically relevant molecules.

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