(4-methyl-4H-1,2,4-triazol-3-yl)methanamine

90%

Reagent Code: #197966
fingerprint
CAS Number 145942-99-0

science Other reagents with same CAS 145942-99-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 112.13 g/mol
Formula C₄H₈N₄
thermostat Physical Properties
Boiling Point 268.3±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.34±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building bioactive molecules. It is also employed in the preparation of agrochemicals and corrosion inhibitors due to its nitrogen-rich heterocyclic affinity. Its amine group facilitates conjugation with other molecular fragments, enhancing its utility in drug design and material science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,170.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4-methyl-4H-1,2,4-triazol-3-yl)methanamine
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building bioactive molecules. It is also employed in the preparation of agrochemicals and corrosion inhibitors due to its nitrogen-rich heterocyclic affinity. Its amine group facilitates conjugation with other molecular fragments, enhancing its utility in drug design and material

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antifungal and anticancer agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building bioactive molecules. It is also employed in the preparation of agrochemicals and corrosion inhibitors due to its nitrogen-rich heterocyclic affinity. Its amine group facilitates conjugation with other molecular fragments, enhancing its utility in drug design and material science.

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...