4-(Methylsulfinyl)benzeneboronic acid

98%

Reagent Code: #90693
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CAS Number 166386-48-7

science Other reagents with same CAS 166386-48-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.02 g/mol
Formula C₇H₉BO₃S
badge Registry Numbers
MDL Number MFCD02093071
thermostat Physical Properties
Boiling Point 416.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the production of pharmaceuticals and agrochemicals. It is particularly valuable in constructing complex aromatic compounds due to its stability and reactivity. Additionally, it serves as a building block in the development of bioactive molecules and materials science research. Its sulfinyl group can also facilitate further functionalization, making it versatile in medicinal chemistry and drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿6,750.00
4-(Methylsulfinyl)benzeneboronic acid
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Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the production of pharmaceuticals and agrochemicals. It is particularly valuable in constructing complex aromatic compounds due to its stability and reactivity. Additionally, it serves as a building block in the development of bioactive molecules and materials science research. Its sulfinyl group can also facilitate further functionalization, making it versatile in

Used in organic synthesis as a key intermediate for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the production of pharmaceuticals and agrochemicals. It is particularly valuable in constructing complex aromatic compounds due to its stability and reactivity. Additionally, it serves as a building block in the development of bioactive molecules and materials science research. Its sulfinyl group can also facilitate further functionalization, making it versatile in medicinal chemistry and drug discovery.

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