5-bromo-1,4-dimethyl-1H-pyrazole

97%

Reagent Code: #197479
fingerprint
CAS Number 1393583-34-0

science Other reagents with same CAS 1393583-34-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.02648 g/mol
Formula C₅H₇BrN₂
badge Registry Numbers
MDL Number MFCD22547955
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and plant growth regulators. Its bromo and methyl functional groups allow for selective cross-coupling reactions, making it valuable in building complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in lead compounds. Also utilized in the preparation of pyrazole-based dyes and functional materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿27,540.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-bromo-1,4-dimethyl-1H-pyrazole
No image available
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and plant growth regulators. Its bromo and methyl functional groups allow for selective cross-coupling reactions, making it valuable in building complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in lead compounds. Also utilized in the
Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and plant growth regulators. Its bromo and methyl functional groups allow for selective cross-coupling reactions, making it valuable in building complex heterocyclic systems. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to enhance binding affinity and metabolic stability in lead compounds. Also utilized in the preparation of pyrazole-based dyes and functional materials.
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...