1,4-Benzenediboronic Acid Bis(pinacol) Ester

97%

Reagent Code: #89439
fingerprint
CAS Number 99770-93-1

science Other reagents with same CAS 99770-93-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Formula C₁₈H₂₈B₂O₄
badge Registry Numbers
MDL Number MFCD08276852
inventory_2 Storage & Handling
Storage room temperature

description Product Description

1,4-Benzenediboronic acid bis(pinacol) ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a preferred reagent for creating biaryl compounds, which are common in drug development and organic electronics. Additionally, it is utilized in the preparation of polymers and functional materials due to its ability to introduce boronic ester groups into molecular structures.

format_list_bulleted Product Specification

Test Parameter Specification
Purity 96.5-100%
Melting Point 241-246
Appearance White to light yellow crystalline solid

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,720.00
inventory 100g
10-20 days ฿19,250.00
inventory 1g
10-20 days ฿500.00
inventory 25g
10-20 days ฿5,980.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1,4-Benzenediboronic Acid Bis(pinacol) Ester
No image available

1,4-Benzenediboronic acid bis(pinacol) ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a preferred reagent for creating biaryl compounds, which are common in drug development and organic electro

1,4-Benzenediboronic acid bis(pinacol) ester is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. It serves as a key building block in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a preferred reagent for creating biaryl compounds, which are common in drug development and organic electronics. Additionally, it is utilized in the preparation of polymers and functional materials due to its ability to introduce boronic ester groups into molecular structures.

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...