6-(Trifluoromethyl)quinazolin-2-amine

97%

Reagent Code: #120414
fingerprint
CAS Number 190273-94-0

science Other reagents with same CAS 190273-94-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.16 g/mol
Formula C₉H₆F₃N₃
badge Registry Numbers
MDL Number MFCD00835296
thermostat Physical Properties
Boiling Point 359.4±52.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition. Its quinazoline core structure is often incorporated into compounds designed to inhibit kinases, which are crucial in regulating cellular processes. This makes it valuable in the development of potential anticancer and anti-inflammatory drugs. Additionally, its trifluoromethyl group enhances the metabolic stability and binding affinity of the resulting molecules, making it a preferred choice for drug discovery efforts. Researchers also explore its applications in creating novel therapeutic agents for treating diseases related to abnormal cell proliferation and immune responses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,043.00
inventory 250mg
10-20 days ฿3,672.00
inventory 1g
10-20 days ฿10,206.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-(Trifluoromethyl)quinazolin-2-amine
No image available

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition. Its quinazoline core structure is often incorporated into compounds designed to inhibit kinases, which are crucial in regulating cellular processes. This makes it valuable in the development of potential anticancer and anti-inflammatory drugs. Additionally, its trifluo

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition. Its quinazoline core structure is often incorporated into compounds designed to inhibit kinases, which are crucial in regulating cellular processes. This makes it valuable in the development of potential anticancer and anti-inflammatory drugs. Additionally, its trifluoromethyl group enhances the metabolic stability and binding affinity of the resulting molecules, making it a preferred choice for drug discovery efforts. Researchers also explore its applications in creating novel therapeutic agents for treating diseases related to abnormal cell proliferation and immune responses.

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...