2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanol

95%

Reagent Code: #89487
fingerprint
CAS Number 1040377-08-9

science Other reagents with same CAS 1040377-08-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.1 g/mol
Formula C₁₁H₁₉BN₂O₃
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of biologically active compounds, such as inhibitors or modulators for various enzymes and receptors, due to its pyrazole moiety. Its applications also extend to material science, where it contributes to the synthesis of organic electronic materials and polymers.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Off-White to Brown Solid
Purity (%) 94.5-100
Water (by Karl Fischer) ≤1.0%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿10,530.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethanol
No image available

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of biologically active compounds, such as inhibitors or modulators for various enzymes and receptors, due to its pyrazole moiety. Its applic

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate. Its boronate ester group enables efficient formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of biologically active compounds, such as inhibitors or modulators for various enzymes and receptors, due to its pyrazole moiety. Its applications also extend to material science, where it contributes to the synthesis of organic electronic materials and polymers.

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...