Ethyl (5E)-6-[1-(4-fluorobenzyl)-1H-pyrrol-2-yl]-2,4-dioxo-5-hexenoate

95%

Reagent Code: #184283
fingerprint
CAS Number 692756-12-0

science Other reagents with same CAS 692756-12-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 343.35 g/mol
Formula C₁₉H₁₈FNO₄
thermostat Physical Properties
Boiling Point 495.8±40.0 °C
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly those targeting cancer-related protein kinases. Its structure supports selective binding and inhibition of specific enzyme pathways involved in tumor growth. Commonly employed in medicinal chemistry for optimizing drug candidates due to its reactive enone and ester functionalities, enabling further chemical modifications. Also utilized in structure-activity relationship (SAR) studies to enhance potency and bioavailability of lead compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿41,610.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl (5E)-6-[1-(4-fluorobenzyl)-1H-pyrrol-2-yl]-2,4-dioxo-5-hexenoate
No image available

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly those targeting cancer-related protein kinases. Its structure supports selective binding and inhibition of specific enzyme pathways involved in tumor growth. Commonly employed in medicinal chemistry for optimizing drug candidates due to its reactive enone and ester functionalities, enabling further chemical modifications. Also utilized in structure-activity relationship (SAR) studies to enhance poten

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly those targeting cancer-related protein kinases. Its structure supports selective binding and inhibition of specific enzyme pathways involved in tumor growth. Commonly employed in medicinal chemistry for optimizing drug candidates due to its reactive enone and ester functionalities, enabling further chemical modifications. Also utilized in structure-activity relationship (SAR) studies to enhance potency and bioavailability of lead compounds.

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...