3-Chloro-4-(4'-fluorobenzyloxy)phenylboronic acid(contains varying amounts of Anhydride)

98%

Reagent Code: #164746
fingerprint
CAS Number 849062-39-1

science Other reagents with same CAS 849062-39-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.5 g/mol
Formula C₁₃H₁₁BClFO₃
badge Registry Numbers
MDL Number MFCD06411358
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing carbon-carbon bonds during drug discovery. Commonly employed in research settings for the preparation of potential anticancer, antiviral, and anti-inflammatory agents. The presence of fluorobenzyloxy and chloro substituents enhances its reactivity and binding selectivity in target molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,650.00
inventory 5g
10-20 days ฿19,770.00
inventory 25g
10-20 days ฿59,320.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Chloro-4-(4'-fluorobenzyloxy)phenylboronic acid(contains varying amounts of Anhydride)
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing carbon-carbon bonds during drug discovery. Commonly employed in research settings for the preparation of potential anticancer, antiviral, and anti-inflammatory agents. The presence of fluorobenzyloxy and chloro

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing carbon-carbon bonds during drug discovery. Commonly employed in research settings for the preparation of potential anticancer, antiviral, and anti-inflammatory agents. The presence of fluorobenzyloxy and chloro substituents enhances its reactivity and binding selectivity in target molecules.

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...