2-((4-Methylpiperidin-1-yl)methyl)phenylboronic acid

98%

Reagent Code: #89603
fingerprint
CAS Number 1313737-75-5

science Other reagents with same CAS 1313737-75-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.12 g/mol
Formula C₁₃H₂₀BNO₂
badge Registry Numbers
MDL Number MFCD16198058
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group is essential for coupling with aryl halides in the presence of a palladium catalyst, making it valuable in the production of biaryl compounds. Additionally, it finds application in the development of materials for organic electronics and as a building block in medicinal chemistry for drug discovery and optimization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿23,750.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-((4-Methylpiperidin-1-yl)methyl)phenylboronic acid
No image available

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group is essential for coupling with aryl halides in the presence of a palladium catalyst, making it valuable in the production of biaryl compounds. Additionally, it finds application in the development of

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group is essential for coupling with aryl halides in the presence of a palladium catalyst, making it valuable in the production of biaryl compounds. Additionally, it finds application in the development of materials for organic electronics and as a building block in medicinal chemistry for drug discovery and optimization.

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...