(2,4-Bis(methoxycarbonyl)phenyl)boronic acid

98%

Reagent Code: #152365
fingerprint
CAS Number 1256354-98-9

science Other reagents with same CAS 1256354-98-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.00 g/mol
Formula C₁₀H₁₁BO₆
badge Registry Numbers
MDL Number MFCD17015764
thermostat Physical Properties
Boiling Point 425.6±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.33±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its dual ester-functionalized structure allows for further derivatization, enabling the construction of highly functionalized biaryl compounds. Commonly employed in the development of specialty polymers and liquid crystals due to its ability to introduce rigid, polar moieties into molecular frameworks. Also utilized in medicinal chemistry for building blocks in drug discovery, where the boronic acid group facilitates selective transformations and the ester groups can be hydrolyzed or reduced to tailor solubility and bioactivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,500.00
inventory 250mg
10-20 days ฿4,120.00
inventory 1g
10-20 days ฿13,300.00
inventory 5g
10-20 days ฿46,460.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2,4-Bis(methoxycarbonyl)phenyl)boronic acid
No image available

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its dual ester-functionalized structure allows for further derivatization, enabling the construction of highly functionalized biaryl compounds. Commonly employed in the development of specialty polymers and liquid crystals due to its ability to introduce rigid, polar moieties into molecular frameworks. Also utilized in medicinal ch

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its dual ester-functionalized structure allows for further derivatization, enabling the construction of highly functionalized biaryl compounds. Commonly employed in the development of specialty polymers and liquid crystals due to its ability to introduce rigid, polar moieties into molecular frameworks. Also utilized in medicinal chemistry for building blocks in drug discovery, where the boronic acid group facilitates selective transformations and the ester groups can be hydrolyzed or reduced to tailor solubility and bioactivity.

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...