N-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide

95%

Reagent Code: #218177
fingerprint
CAS Number 945863-21-8

science Other reagents with same CAS 945863-21-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.11 g/mol
Formula C₁₃H₁₉BN₂O₃
badge Registry Numbers
MDL Number MFCD08458483
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl halides under mild conditions, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the picolinamide moiety enhances stability and can assist in directing metalation or improving solubility during synthetic transformations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿860.00
250mg
10-20 days ฿1,330.00
1g
10-20 days ฿3,960.00
5g
10-20 days ฿18,300.00
10g
10-20 days ฿32,500.00
N-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide
No image available
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl halides under mild conditions, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the picolinamide moiety enhances stability and can assist in directing metalation or improving solubility during s
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl halides under mild conditions, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The presence of the picolinamide moiety enhances stability and can assist in directing metalation or improving solubility during synthetic transformations.
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...