3-BROMO-5-(METHOXYCARBONYL)BENZENEBORONIC ACID

95%

Reagent Code: #91986
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CAS Number 913835-87-7

science Other reagents with same CAS 913835-87-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.8617 g/mol
Formula C₈H₈BBrO₄
thermostat Physical Properties
Boiling Point 410.9 ℃ at 760 mmHg
inventory_2 Storage & Handling
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description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its methoxycarbonyl group can act as a functional handle for further chemical modifications, enhancing its versatility in synthetic applications. Its stability and reactivity make it a preferred choice in medicinal chemistry for developing drug candidates and biologically active compounds.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,952.00
inventory 100mg
10-20 days ฿6,192.00
inventory 500mg
10-20 days ฿20,592.00

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3-BROMO-5-(METHOXYCARBONYL)BENZENEBORONIC ACID
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its methoxycarbonyl group can act as a functional handle for further ch

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating complex organic molecules. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its methoxycarbonyl group can act as a functional handle for further chemical modifications, enhancing its versatility in synthetic applications. Its stability and reactivity make it a preferred choice in medicinal chemistry for developing drug candidates and biologically active compounds.

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