(4-((Cyanomethyl)carbamoyl)phenyl)boronic acid

97%

Reagent Code: #90652
fingerprint
CAS Number 1056636-11-3

science Other reagents with same CAS 1056636-11-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.99 g/mol
Formula C₉H₉BN₂O₃
badge Registry Numbers
MDL Number MFCD24566607
inventory_2 Storage & Handling
Density 1.31±0.1 g/cm3(Predicted)
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the coupling of aryl or vinyl halides with aryl boronic acids to produce biaryl compounds, which are valuable intermediates in pharmaceuticals, agrochemicals, and materials science. Additionally, its structure, featuring a boronic acid group and a cyanomethyl carbamoyl moiety, makes it suitable for applications in medicinal chemistry, where it can be used to design and synthesize biologically active molecules. Its ability to interact with diols and other functional groups also makes it relevant in the development of sensors and diagnostic tools.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,728.00
inventory 250mg
10-20 days ฿2,079.00
inventory 1g
10-20 days ฿8,154.00
inventory 5g
10-20 days ฿17,757.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4-((Cyanomethyl)carbamoyl)phenyl)boronic acid
No image available

This compound is primarily utilized in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the coupling of aryl or vinyl halides with aryl boronic acids to produce biaryl compounds, which are valuable intermediates in pharmaceuticals, agrochemicals, and materials science. Additionally, its structure, featuring a boronic acid group and a cyanomethyl carbamoyl moiety, makes it suitable for app

This compound is primarily utilized in organic synthesis, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the coupling of aryl or vinyl halides with aryl boronic acids to produce biaryl compounds, which are valuable intermediates in pharmaceuticals, agrochemicals, and materials science. Additionally, its structure, featuring a boronic acid group and a cyanomethyl carbamoyl moiety, makes it suitable for applications in medicinal chemistry, where it can be used to design and synthesize biologically active molecules. Its ability to interact with diols and other functional groups also makes it relevant in the development of sensors and diagnostic tools.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...