4-Isopropoxy-3-methylphenylboronic acid

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Reagent Code: #86120
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CAS Number 850568-09-1

science Other reagents with same CAS 850568-09-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.04 g/mol
Formula C₁₀H₁₅BO₃
badge Registry Numbers
MDL Number MFCD06659871
thermostat Physical Properties
Boiling Point 338.297°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it is utilized in the development of materials for electronic devices and sensors due to its ability to form stable bonds with various organic substrates. Its applications also extend to research in medicinal chemistry, where it aids in the synthesis of potential drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,012.50
inventory 1g
10-20 days ฿3,037.50
inventory 5g
10-20 days ฿12,150.00
inventory 10g
10-20 days ฿23,962.50

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4-Isopropoxy-3-methylphenylboronic acid
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it is utilized in the development of materials for electronic devices and sensors due to its ability to form stable

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it is utilized in the development of materials for electronic devices and sensors due to its ability to form stable bonds with various organic substrates. Its applications also extend to research in medicinal chemistry, where it aids in the synthesis of potential drug candidates.

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