4-Methyl-3-Nitrophenylboronic Acid

≥98%

Reagent Code: #90680
fingerprint
CAS Number 80500-27-2

science Other reagents with same CAS 80500-27-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.95 g/mol
Formula C₇H₈BNO₄
badge Registry Numbers
MDL Number MFCD00191550
thermostat Physical Properties
Melting Point 265-270 °C
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

4-Methyl-3-Nitrophenylboronic Acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, which is a fundamental process in creating complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the production of various bioactive compounds and fine chemicals. Its boronic acid group makes it highly reactive and suitable for coupling with aryl halides, enabling the synthesis of biaryl structures. Additionally, it is utilized in the development of sensors and probes for detecting specific molecules in biochemical research. Its nitro and methyl substituents further enhance its reactivity and selectivity in diverse chemical transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,710.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Methyl-3-Nitrophenylboronic Acid
No image available

4-Methyl-3-Nitrophenylboronic Acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, which is a fundamental process in creating complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the production of various bioactive compounds and fine chemicals. Its boronic acid group makes it highly reactive and suitable for coupling

4-Methyl-3-Nitrophenylboronic Acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, which is a fundamental process in creating complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the production of various bioactive compounds and fine chemicals. Its boronic acid group makes it highly reactive and suitable for coupling with aryl halides, enabling the synthesis of biaryl structures. Additionally, it is utilized in the development of sensors and probes for detecting specific molecules in biochemical research. Its nitro and methyl substituents further enhance its reactivity and selectivity in diverse chemical transformations.

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...