6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-amine

95%

Reagent Code: #196491
fingerprint
CAS Number 1448427-99-3

science Other reagents with same CAS 1448427-99-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.2442 g/mol
Formula C₁₀H₁₃N₅
badge Registry Numbers
MDL Number MFCD24127938
thermostat Physical Properties
Boiling Point 405.8±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.279±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof storage, dry seal

description Product Description

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in pharmaceuticals targeting cancer pathways. It shows utility in developing drugs that modulate protein kinases involved in cell proliferation and inflammation. Its structure enables strong binding to enzyme active sites, enhancing therapeutic potency. Also employed in research for designing novel antitumor agents due to its ability to mimic purine scaffolds in nucleotide-binding proteins.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,120.00
inventory 250mg
10-20 days ฿1,930.00
inventory 1g
10-20 days ฿5,390.00
inventory 5g
10-20 days ฿25,630.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-(4-isopropyl-4H-1,2,4-triazol-3-yl)pyridin-2-amine
No image available

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in pharmaceuticals targeting cancer pathways. It shows utility in developing drugs that modulate protein kinases involved in cell proliferation and inflammation. Its structure enables strong binding to enzyme active sites, enhancing therapeutic potency. Also employed in research for designing novel antitumor agents due to its ability to mimic purine scaffolds in nucleotide-binding proteins.

Used as a key intermediate in the synthesis of kinase inhibitors, particularly in pharmaceuticals targeting cancer pathways. It shows utility in developing drugs that modulate protein kinases involved in cell proliferation and inflammation. Its structure enables strong binding to enzyme active sites, enhancing therapeutic potency. Also employed in research for designing novel antitumor agents due to its ability to mimic purine scaffolds in nucleotide-binding proteins.

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...