(3-((Methylamino)methyl)phenyl)boronic acid

≥95%

Reagent Code: #209165
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CAS Number 1146614-39-2

science Other reagents with same CAS 1146614-39-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.00 g/mol
Formula C₈H₁₂BNO₂
badge Registry Numbers
MDL Number MFCD18453453
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in research settings for designing enzyme inhibitors, especially those targeting serine proteases. Also utilized in the preparation of boron-containing compounds for potential use in neutron capture therapy and biosensors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,330.00
inventory 250mg
10-20 days ฿6,660.00
inventory 1g
10-20 days ฿23,300.00

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(3-((Methylamino)methyl)phenyl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in research settings for designing enzyme inhibitors, especially those targeting serine proteases. Also utilized in the preparation of boron-c

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in research settings for designing enzyme inhibitors, especially those targeting serine proteases. Also utilized in the preparation of boron-containing compounds for potential use in neutron capture therapy and biosensors.

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