6-Nitroindolin-2-one

≥95%

Reagent Code: #218154
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CAS Number 474799-41-2

science Other reagents with same CAS 474799-41-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 178.15 g/mol
Formula C₈H₆N₂O₃
badge Registry Numbers
MDL Number MFCD09835636
thermostat Physical Properties
Boiling Point 390.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, 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 substitutions on the aromatic ring and nitrogen functionalities. Also employed in the preparation of fluorescent probes and dyes owing to its electron-withdrawing nitro group and conjugated structure. Its derivatives show potential in biological assays targeting inflammatory and neurodegenerative diseases.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,890.00
1g
10-20 days ฿4,840.00
5g
10-20 days ฿19,200.00
25g
10-20 days ฿91,110.00
6-Nitroindolin-2-one
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Used as an intermediate in the synthesis of pharmaceuticals, 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 substitutions on the aromatic ring and nitrogen functionalities. Also employed in the preparation of fluorescent probes and dyes owing to its electron-withdrawing nitro group and conjugated structure. Its derivatives show potential in biological assays targeting inflammatory and

Used as an intermediate in the synthesis of pharmaceuticals, 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 substitutions on the aromatic ring and nitrogen functionalities. Also employed in the preparation of fluorescent probes and dyes owing to its electron-withdrawing nitro group and conjugated structure. Its derivatives show potential in biological assays targeting inflammatory and neurodegenerative diseases.

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