1-(4-tert-Butylphenyl)-1H-pyrazole-4-boronic acid

95%

Reagent Code: #89472
fingerprint
CAS Number 2225169-39-9

science Other reagents with same CAS 2225169-39-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.09728 g/mol
Formula C₁₃H₁₇BN₂O₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry, where it aids in the development of drug candidates. Its boronic acid group allows for efficient coupling with aryl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, such as inhibitors or receptor modulators. Additionally, it is utilized in material science for the preparation of advanced polymers and organic electronic materials, contributing to the development of OLEDs and other optoelectronic devices. Its stability and reactivity make it a versatile reagent in both academic research and industrial applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿5,634.00
inventory 25mg
10-20 days ฿16,884.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-(4-tert-Butylphenyl)-1H-pyrazole-4-boronic acid
No image available

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry, where it aids in the development of drug candidates. Its boronic acid group allows for efficient coupling with aryl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, such as inhibitors or receptor modulat

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, especially in the pharmaceutical industry, where it aids in the development of drug candidates. Its boronic acid group allows for efficient coupling with aryl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, such as inhibitors or receptor modulators. Additionally, it is utilized in material science for the preparation of advanced polymers and organic electronic materials, contributing to the development of OLEDs and other optoelectronic devices. Its stability and reactivity make it a versatile reagent in both academic research and industrial applications.

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...