3-(m-tolyl)-1H-pyrazol-5-amine

95%

Reagent Code: #196489
fingerprint
CAS Number 80568-96-3

science Other reagents with same CAS 80568-96-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.21 g/mol
Formula C₁₀H₁₁N₃
badge Registry Numbers
MDL Number MFCD02664271
thermostat Physical Properties
Melting Point 86-89 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, 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 engage in aromatic interactions, enhancing binding affinity to target proteins. Also employed in the preparation of agrochemicals and bioactive molecules with anti-inflammatory properties. Its structural features make it valuable in optimizing lead compounds during drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,860.00
inventory 250mg
10-20 days ฿4,790.00
inventory 1g
10-20 days ฿11,680.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-(m-tolyl)-1H-pyrazol-5-amine
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, 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 engage in aromatic interactions, enhancing binding affinity to target proteins. Also employed in the preparation of agrochemicals and bioactive molecules with anti-inflammatory properties. Its structural features make it valuable in optimizing lead compounds dur

Used as a key intermediate in the synthesis of pharmaceutical compounds, 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 engage in aromatic interactions, enhancing binding affinity to target proteins. Also employed in the preparation of agrochemicals and bioactive molecules with anti-inflammatory properties. Its structural features make it valuable in optimizing lead compounds during 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...