3-cyanophenylboronic acid-1,3-propanediol ester

98%

Reagent Code: #161753
fingerprint
CAS Number 684648-40-6

science Other reagents with same CAS 684648-40-6

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical and agrochemical development. Its boronic ester structure enhances stability and handling compared to the free boronic acid, making it suitable for solid-phase synthesis and combinatorial chemistry. Commonly employed in the preparation of drug candidates targeting kinase inhibition and central nervous system disorders. Also utilized in the fabrication of sensors and functional materials due to its selective reactivity with diols and electrophilic partners.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,120.00
inventory 1g
10-20 days ฿5,430.00
inventory 5g
10-20 days ฿19,650.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-cyanophenylboronic acid-1,3-propanediol ester
No image available

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical and agrochemical development. Its boronic ester structure enhances stability and handling compared to the free boronic acid, making it suitable for solid-phase synthesis and combinatorial chemistry. Commonly employed in the preparation of drug candidates targeting kinase inhibition and central nervous system disorders. Also utilized in the fabrication of sensors and

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex biaryl compounds in pharmaceutical and agrochemical development. Its boronic ester structure enhances stability and handling compared to the free boronic acid, making it suitable for solid-phase synthesis and combinatorial chemistry. Commonly employed in the preparation of drug candidates targeting kinase inhibition and central nervous system disorders. Also utilized in the fabrication of sensors and functional materials due to its selective reactivity with diols and electrophilic partners.

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...