7-Chloro-6-hydroxy-1h-indole-3-carbaldehyde

98%

Reagent Code: #156740
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CAS Number 1227575-94-1

science Other reagents with same CAS 1227575-94-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.6 g/mol
Formula C₉H₆ClNO₂
thermostat Physical Properties
Boiling Point 424.5±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.578±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives with potential neurological and anti-inflammatory activity. Commonly employed in research settings to construct complex heterocyclic systems. Also utilized in the preparation of fluorescent probes due to its aldehyde and hydroxyl functional groups, enabling conjugation and sensor design. Shows promise in medicinal chemistry for designing serotonin receptor modulators.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿9,530.00
50mg
10-20 days ฿16,180.00
100mg
10-20 days ฿27,500.00
7-Chloro-6-hydroxy-1h-indole-3-carbaldehyde
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Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives with potential neurological and anti-inflammatory activity. Commonly employed in research settings to construct complex heterocyclic systems. Also utilized in the preparation of fluorescent probes due to its aldehyde and hydroxyl functional groups, enabling conjugation and sensor design. Shows promise in medicinal chemistry for designing serotonin re

Used in organic synthesis as an intermediate for pharmaceuticals and bioactive compounds. Its structure supports the development of indole-based derivatives with potential neurological and anti-inflammatory activity. Commonly employed in research settings to construct complex heterocyclic systems. Also utilized in the preparation of fluorescent probes due to its aldehyde and hydroxyl functional groups, enabling conjugation and sensor design. Shows promise in medicinal chemistry for designing serotonin receptor modulators.

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