4-Bromo-2,6-difluorophenylboronic acid

95%

Reagent Code: #90660
fingerprint
CAS Number 352535-81-0

science Other reagents with same CAS 352535-81-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.81 g/mol
Formula C₆H₄BBrF₂O₂
badge Registry Numbers
MDL Number MFCD03095369
thermostat Physical Properties
Melting Point 155-160°C
Boiling Point 298.4°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in the pharmaceutical industry for drug development. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable in constructing biaryl compounds. Additionally, it is utilized in materials science for designing advanced polymers and electronic materials. Its specific fluorine and bromine substituents enhance its reactivity and selectivity in various chemical transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿414.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Bromo-2,6-difluorophenylboronic acid
No image available

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in the pharmaceutical industry for drug development. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable in constructing biaryl compounds. Additionally, it is utilized in materials science for designing advanced polymers and electronic materials. Its specific fluorine and bro

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in the pharmaceutical industry for drug development. Its boronic acid group enables it to form carbon-carbon bonds efficiently, making it valuable in constructing biaryl compounds. Additionally, it is utilized in materials science for designing advanced polymers and electronic materials. Its specific fluorine and bromine substituents enhance its reactivity and selectivity in various 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...