4-Bromo-1-phenyl-1H-pyrazole

97%

Reagent Code: #145269
fingerprint
CAS Number 15115-52-3

science Other reagents with same CAS 15115-52-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.07 g/mol
Formula C₉H₇BrN₂
badge Registry Numbers
MDL Number MFCD00234505
thermostat Physical Properties
Boiling Point 296.3°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with anti-inflammatory, antimicrobial, and anticancer properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of more complex pyrazole derivatives. It is also employed in cross-coupling reactions, such as Suzuki and Heck reactions, to form carbon-carbon bonds for drug discovery and material science applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿290.00
inventory 1g
10-20 days ฿640.00
inventory 5g
10-20 days ฿2,420.00
inventory 100g
10-20 days ฿40,010.00
inventory 25g
10-20 days ฿10,420.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Bromo-1-phenyl-1H-pyrazole
No image available

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with anti-inflammatory, antimicrobial, and anticancer properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of more complex pyrazole derivatives. It is also employed in cross-coupling reactions, such as Suzuki and Heck reactions, to form carbon-carbon bonds for drug discovery and material science applications.

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with anti-inflammatory, antimicrobial, and anticancer properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of more complex pyrazole derivatives. It is also employed in cross-coupling reactions, such as Suzuki and Heck reactions, to form carbon-carbon bonds for drug discovery and material science applications.

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...