4,4,5,5-Tetramethyl-2-(p-tolyl)-1,3,2-dioxaborolane

98%

Reagent Code: #90302
fingerprint
CAS Number 195062-57-8

science Other reagents with same CAS 195062-57-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.10 g/mol
Formula C₁₃H₁₉BO₂
badge Registry Numbers
MDL Number MFCD03453662
thermostat Physical Properties
Melting Point 52.0 to 56.0 deg-C
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester structure provides stability to the boronic acid functionality, making it a valuable reagent for forming carbon-carbon bonds and enabling the construction of complex organic molecules. Its stability and reactivity make it suitable for use in various catalytic processes, contributing to the development of novel compounds in drug discovery and material science.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 97.5-100%
Appearance White to off-white crystalline powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿820.00
inventory 1g
10-20 days ฿300.00
inventory 25g
10-20 days ฿3,320.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4,4,5,5-Tetramethyl-2-(p-tolyl)-1,3,2-dioxaborolane
No image available

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester structure provides stability to the boronic acid functionality, making it a valuable reagent for forming carbon-carbon bonds and enabling the construction of complex organic molecules. Its stability and reactivity make it suitable for use in various catalytic processes, contributi

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester structure provides stability to the boronic acid functionality, making it a valuable reagent for forming carbon-carbon bonds and enabling the construction of complex organic molecules. Its stability and reactivity make it suitable for use in various catalytic processes, contributing to the development of novel compounds in drug discovery and material science.

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...