(4-((2-Ethoxy-2-oxoethyl)carbamoyl)phenyl)boronic acid

98%

Reagent Code: #113262
fingerprint
CAS Number 1072946-08-7

science Other reagents with same CAS 1072946-08-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.04 g/mol
Formula C₁₁H₁₄BNO₅
badge Registry Numbers
MDL Number MFCD09972113
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its structure allows for efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it is employed in the development of bioactive compounds and materials science research, where precise molecular construction is essential.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,232.00
inventory 1g
10-20 days ฿5,958.00
inventory 5g
10-20 days ฿19,179.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4-((2-Ethoxy-2-oxoethyl)carbamoyl)phenyl)boronic acid
No image available

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its structure allows for efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it is employed in the development of bioactive compounds and

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic acid derivative, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its structure allows for efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it is employed in the development of bioactive compounds and materials science research, where precise molecular construction is essential.

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...