(5-bromo-1H-indol-2-yl)methanol

95%

Reagent Code: #196007
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CAS Number 53590-48-0

science Other reagents with same CAS 53590-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.07 g/mol
Formula C₉H₈BrNO
badge Registry Numbers
MDL Number MFCD08689788
thermostat Physical Properties
Melting Point 110-115 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Particularly valuable in the development of serotonin receptor modulators and kinase inhibitors due to the indole scaffold. The bromo substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex molecules. Also explored in medicinal chemistry for the design of anti-inflammatory and anticancer agents. The hydroxymethyl group can be easily modified to esters, ethers, or aldehydes, increasing its utility in drug discovery research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,700.00
inventory 250mg
10-20 days ฿9,250.00
inventory 1g
10-20 days ฿14,450.00
inventory 5g
10-20 days ฿58,940.00

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(5-bromo-1H-indol-2-yl)methanol
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Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Particularly valuable in the development of serotonin receptor modulators and kinase inhibitors due to the indole scaffold. The bromo substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex molecules. Also explored in medicinal chemistry for the design of anti-inflammatory and anticancer agents. The hydroxymethyl g

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Particularly valuable in the development of serotonin receptor modulators and kinase inhibitors due to the indole scaffold. The bromo substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex molecules. Also explored in medicinal chemistry for the design of anti-inflammatory and anticancer agents. The hydroxymethyl group can be easily modified to esters, ethers, or aldehydes, increasing its utility in drug discovery research.

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