Indolin-6-ol

≥95%

Reagent Code: #200213
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CAS Number 4770-37-0

science Other reagents with same CAS 4770-37-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.16 g/mol
Formula C₈H₉NO
badge Registry Numbers
MDL Number MFCD11559070
thermostat Physical Properties
Boiling Point 302.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Indolin-6-ol is primarily used as an intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its structure supports the development of kinase inhibitors and neuroprotective agents, making it valuable in medicinal chemistry research. It is also employed in the creation of dyes and fluorescent probes due to its aromatic and electron-donating properties, which enhance optical characteristics. Additionally, derivatives of indolin-6-ol appear in the development of antioxidants and anti-inflammatory agents, where the hydroxyl group contributes to radical scavenging activity. Its versatility in ring functionalization allows for tailored modifications in drug design and materials science.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,810.00
inventory 250mg
10-20 days ฿5,700.00
inventory 1g
10-20 days ฿15,800.00

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Indolin-6-ol
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Indolin-6-ol is primarily used as an intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its structure supports the development of kinase inhibitors and neuroprotective agents, making it valuable in medicinal chemistry research. It is also employed in the creation of dyes and fluorescent probes due to its aromatic and electron-donating properties, which enhance optical characteristics. Additionally, derivatives of indolin-6-ol appear in the development of antioxidants and

Indolin-6-ol is primarily used as an intermediate in the synthesis of pharmaceuticals and biologically active compounds. Its structure supports the development of kinase inhibitors and neuroprotective agents, making it valuable in medicinal chemistry research. It is also employed in the creation of dyes and fluorescent probes due to its aromatic and electron-donating properties, which enhance optical characteristics. Additionally, derivatives of indolin-6-ol appear in the development of antioxidants and anti-inflammatory agents, where the hydroxyl group contributes to radical scavenging activity. Its versatility in ring functionalization allows for tailored modifications in drug design and materials science.

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