3-(Butylaminocarbonyl)phenylboronic acid(contains varying amounts of Anhydride)

98%

Reagent Code: #117537
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CAS Number 397843-70-8

science Other reagents with same CAS 397843-70-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.06 g/mol
Formula C₁₁H₁₆BNO₃
badge Registry Numbers
MDL Number MFCD04115691
thermostat Physical Properties
Melting Point 216-224°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting specific enzymes or receptors. It plays a role in organic synthesis, especially in cross-coupling reactions such as the Suzuki-Miyaura coupling, where it facilitates the formation of carbon-carbon bonds. This compound is also employed in the preparation of boron-containing materials, which are useful in various industrial applications, including polymers and coatings. Additionally, it is utilized in research settings for studying boronic acid derivatives and their interactions with biological molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,016.00
inventory 1g
10-20 days ฿3,672.00
inventory 5g
10-20 days ฿8,847.00

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3-(Butylaminocarbonyl)phenylboronic acid(contains varying amounts of Anhydride)
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting specific enzymes or receptors. It plays a role in organic synthesis, especially in cross-coupling reactions such as the Suzuki-Miyaura coupling, where it facilitates the formation of carbon-carbon bonds. This compound is also employed in the preparation of boron-containing materials, which are useful in various industrial applications, including polymers and coatings. Additionally, it

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting specific enzymes or receptors. It plays a role in organic synthesis, especially in cross-coupling reactions such as the Suzuki-Miyaura coupling, where it facilitates the formation of carbon-carbon bonds. This compound is also employed in the preparation of boron-containing materials, which are useful in various industrial applications, including polymers and coatings. Additionally, it is utilized in research settings for studying boronic acid derivatives and their interactions with biological molecules.

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