Propanoic acid, 3-[(5-bromo-2-fluorophenyl)amino]-2,2-dimethyl-3-oxo-, methyl ester

≥95%

Reagent Code: #223349
fingerprint
CAS Number 1890113-34-4

science Other reagents with same CAS 1890113-34-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 318.1389 g/mol
Formula C₁₂H₁₃BrFNO₃
badge Registry Numbers
MDL Number MFCD31556113
thermostat Physical Properties
Boiling Point 405.1±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.497±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure, featuring bromine and fluorine substituents, supports binding to specific enzyme targets, enhancing stability and selectivity. This makes it valuable in medicinal chemistry for designing drugs with high potency. Also employed in research settings to explore new bioactive molecules and optimize lead compounds during drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,200.00
inventory 250mg
10-20 days ฿32,000.00
inventory 1g
10-20 days ฿64,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Propanoic acid, 3-[(5-bromo-2-fluorophenyl)amino]-2,2-dimethyl-3-oxo-, methyl ester
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure, featuring bromine and fluorine substituents, supports binding to specific enzyme targets, enhancing stability and selectivity. This makes it valuable in medicinal chemistry for designing drugs with high potency. Also employed in research settings to explore new bioactive molecules and optimize lead compounds during drug discovery.

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure, featuring bromine and fluorine substituents, supports binding to specific enzyme targets, enhancing stability and selectivity. This makes it valuable in medicinal chemistry for designing drugs with high potency. Also employed in research settings to explore new bioactive molecules and optimize 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...