3-PICOLINE-4-BORONIC ACID HCL

95%

Reagent Code: #91985
fingerprint
CAS Number 1072952-40-9

science Other reagents with same CAS 1072952-40-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.41 g/mol
Formula C₆H₉BClNO₂
badge Registry Numbers
MDL Number MFCD06659519
inventory_2 Storage & Handling
Storage -20℃

description Product Description

3-Picoline-4-boronic acid HCl is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for constructing carbon-carbon bonds, enabling the synthesis of complex molecules, including drug intermediates and active pharmaceutical ingredients (APIs). Its boronic acid group acts as a key functional moiety, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it serves as a building block in the development of agrochemicals, fine chemicals, and materials science research, where precise molecular assembly is required. Its stability and reactivity make it a valuable reagent in medicinal chemistry for designing and optimizing drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿16,092.00
inventory 10mg
10-20 days ฿7,992.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-PICOLINE-4-BORONIC ACID HCL
No image available
3-Picoline-4-boronic acid HCl is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for constructing carbon-carbon bonds, enabling the synthesis of complex molecules, including drug intermediates and active pharmaceutical ingredients (APIs). Its boronic acid group acts as a key functional moiety, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. Additionally, it serves as a building block in the development of agrochemicals, fine chemicals, and materials science research, where precise molecular assembly is required. Its stability and reactivity make it a valuable reagent in medicinal chemistry for designing and optimizing drug candidates.
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...