(2-methyl-4-morpholinophenyl)boronic acid

95%

Reagent Code: #58158
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CAS Number 2225175-77-7

science Other reagents with same CAS 2225175-77-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.06064 g/mol
Formula C₁₁H₁₆BNO₃
inventory_2 Storage & Handling
Storage -20℃

description Product Description

(2-methyl-4-morpholinophenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate in the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it is employed in the development of bioactive molecules and drug candidates, contributing to medicinal chemistry research. Its stability and reactivity also make it suitable for use in catalytic processes and polymer chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10mg
10-20 days ฿11,592.00
25mg
10-20 days ฿23,292.00
(2-methyl-4-morpholinophenyl)boronic acid
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(2-methyl-4-morpholinophenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate in the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it is employed in

(2-methyl-4-morpholinophenyl)boronic acid is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This compound serves as a key intermediate in the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it is employed in the development of bioactive molecules and drug candidates, contributing to medicinal chemistry research. Its stability and reactivity also make it suitable for use in catalytic processes and polymer chemistry.

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