(3-(tert-Butylcarbamoyl)-4-chlorophenyl)boronic acid

97%

Reagent Code: #154435
fingerprint
CAS Number 871332-72-8

science Other reagents with same CAS 871332-72-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.51 g/mol
Formula C₁₁H₁₅BClNO₃
badge Registry Numbers
MDL Number MFCD07783864
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The tert-butylcarbamoyl and chloro substituents provide steric and electronic properties that enhance selectivity in coupling reactions. Commonly employed in the development of kinase inhibitors and other bioactive molecules in medicinal chemistry research. Also utilized in the synthesis of functional materials and ligands for catalysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,580.00
inventory 1g
10-20 days ฿11,460.00
inventory 5g
10-20 days ฿34,380.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3-(tert-Butylcarbamoyl)-4-chlorophenyl)boronic acid
No image available

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The tert-butylcarbamoyl and chloro substituents provide steric and electronic properties that enhance selectivity in coupling reactions. Commonly employed in the development of kinase inhibitors and other bioactive molecules in medicinal chemistry r

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The tert-butylcarbamoyl and chloro substituents provide steric and electronic properties that enhance selectivity in coupling reactions. Commonly employed in the development of kinase inhibitors and other bioactive molecules in medicinal chemistry research. Also utilized in the synthesis of functional materials and ligands for catalysis.

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...