7-Nitro-1,3-dihydro-2H-indol-2-one

≥95%

Reagent Code: #218022
fingerprint
CAS Number 25369-31-7

science Other reagents with same CAS 25369-31-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.1448 g/mol
Formula C₈H₆N₂O₃
badge Registry Numbers
MDL Number MFCD04088356
thermostat Physical Properties
Boiling Point 392.5℃ at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8℃, dry, sealed

description Product Description

Used as an 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 ability to undergo selective functionalization on the aromatic ring and lactam nitrogen. Commonly employed in research settings to design bioactive molecules targeting neurological disorders and inflammatory diseases. Also utilized in the preparation of fluorescent probes for biochemical assays owing to its nitro group’s electron-withdrawing properties and inherent ring structure favorable for conjugation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,240.00
inventory 1g
10-20 days ฿14,970.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
7-Nitro-1,3-dihydro-2H-indol-2-one
No image available

Used as an 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 ability to undergo selective functionalization on the aromatic ring and lactam nitrogen. Commonly employed in research settings to design bioactive molecules targeting neurological disorders and inflammatory diseases. Also utilized in the preparation of fluorescent probes for biochemical assays owin

Used as an 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 ability to undergo selective functionalization on the aromatic ring and lactam nitrogen. Commonly employed in research settings to design bioactive molecules targeting neurological disorders and inflammatory diseases. Also utilized in the preparation of fluorescent probes for biochemical assays owing to its nitro group’s electron-withdrawing properties and inherent ring structure favorable for conjugation.

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...