3-(4-Bromophenyl)-1H-pyrazole

≥98%

Reagent Code: #146994
fingerprint
CAS Number 73387-46-9

science Other reagents with same CAS 73387-46-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.07 g/mol
Formula C₉H₇BrN₂
badge Registry Numbers
MDL Number MFCD01940434
thermostat Physical Properties
Melting Point 132-136ºC
Boiling Point 388.9ºC
inventory_2 Storage & Handling
Density 1.565 g/cm3
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and anticancer agents. Its structure supports the creation of more complex molecules with biological activity. Commonly employed in medicinal chemistry for constructing pyrazole-based drug candidates. Also utilized in agrochemical research for designing new pesticides and herbicides due to its favorable reactivity and stability. Serves as a building block in organic synthesis, especially in cross-coupling reactions to form biaryl compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿360.00
inventory 5g
10-20 days ฿870.00
inventory 25g
10-20 days ฿3,270.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-(4-Bromophenyl)-1H-pyrazole
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and anticancer agents. Its structure supports the creation of more complex molecules with biological activity. Commonly employed in medicinal chemistry for constructing pyrazole-based drug candidates. Also utilized in agrochemical research for designing new pesticides and herbicides due to its favorable reactivity and stability. Serves as a building block in organic synthesis, especially i

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and anticancer agents. Its structure supports the creation of more complex molecules with biological activity. Commonly employed in medicinal chemistry for constructing pyrazole-based drug candidates. Also utilized in agrochemical research for designing new pesticides and herbicides due to its favorable reactivity and stability. Serves as a building block in organic synthesis, especially in cross-coupling reactions to form biaryl compounds.

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...