5-Benzyl-1H-pyrazol-3-amine

97%

Reagent Code: #148219
fingerprint
CAS Number 150712-24-6

science Other reagents with same CAS 150712-24-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.21 g/mol
Formula C₁₀H₁₁N₃
badge Registry Numbers
MDL Number MFCD09991902
thermostat Physical Properties
Boiling Point 405.316°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and participate in π-π stacking interactions, enhancing binding affinity to target proteins. Also employed in the preparation of agrochemicals and functional materials where nitrogen-rich heterocycles are required. Its structural features make it suitable for use in combinatorial chemistry and high-throughput screening for drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,460.00
inventory 250mg
10-20 days ฿6,810.00
inventory 1g
10-20 days ฿16,890.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Benzyl-1H-pyrazol-3-amine
No image available
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and participate in π-π stacking interactions, enhancing binding affinity to target proteins. Also employed in the preparation of agrochemicals and functional materials where nitrogen-rich heterocycles are required. Its structural features make it suitable for use in combinatori
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and participate in π-π stacking interactions, enhancing binding affinity to target proteins. Also employed in the preparation of agrochemicals and functional materials where nitrogen-rich heterocycles are required. Its structural features make it suitable for use in combinatorial chemistry and high-throughput screening for drug discovery.
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...