2-(3,5-Dinitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #174671
fingerprint
CAS Number 428820-95-5

science Other reagents with same CAS 428820-95-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.07 g/mol
Formula C₁₂H₁₅BN₂O₆
badge Registry Numbers
MDL Number MFCD11504965
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. It serves as a stable boronic ester derivative, facilitating the preparation of biaryl compounds which are common structural motifs in pharmaceuticals, agrochemicals, and functional materials. Its dinitrophenyl group enhances reactivity and can act as a directing or activating group in further transformations. Commonly employed in medicinal chemistry for building complex aromatic frameworks under mild conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿3,810.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(3,5-Dinitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
No image available
Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. It serves as a stable boronic ester derivative, facilitating the preparation of biaryl compounds which are common structural motifs in pharmaceuticals, agrochemicals, and functional materials. Its dinitrophenyl group enhances reactivity and can act as a directing or activating group in further transformations. Commonly employed in medicinal chemistry for building complex aromatic frameworks under mild conditions.
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...