5-Bromo-3-ethylindolin-2-one

97%

Reagent Code: #153265
fingerprint
CAS Number 304876-05-9

science Other reagents with same CAS 304876-05-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.1 g/mol
Formula C₁₀H₁₀BrNO
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its indolinone scaffold, which is known for biological activity in cell signaling pathways. Commonly employed in the preparation of tyrosine kinase and cyclin-dependent kinase inhibitors. Also utilized in research settings for structure-activity relationship (SAR) studies to optimize drug candidates. Its bromo functionality allows for further derivatization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid generation of compound libraries for drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,320.00
inventory 250mg
10-20 days ฿3,240.00
inventory 1g
10-20 days ฿12,870.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Bromo-3-ethylindolin-2-one
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its indolinone scaffold, which is known for biological activity in cell signaling pathways. Commonly employed in the preparation of tyrosine kinase and cyclin-dependent kinase inhibitors. Also utilized in research settings for structure-activity relationship (SAR) studies to optimize drug candidates.

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its indolinone scaffold, which is known for biological activity in cell signaling pathways. Commonly employed in the preparation of tyrosine kinase and cyclin-dependent kinase inhibitors. Also utilized in research settings for structure-activity relationship (SAR) studies to optimize drug candidates. Its bromo functionality allows for further derivatization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid generation of compound libraries for 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...