Methyl 6-bromo-2-methyl-1H-indole-3-carboxylate

≥95%

Reagent Code: #202997
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CAS Number 1313753-18-2

science Other reagents with same CAS 1313753-18-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.11 g/mol
Formula C₁₁H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD23159658
thermostat Physical Properties
Boiling Point 384.3±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.556±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its structure supports the construction of complex indole-based molecules with biological activity. Commonly employed in medicinal chemistry for creating analogs in drug discovery programs targeting neurological disorders and inflammation. Also utilized in research settings to prepare fluorescent probes and labeled compounds for biochemical assays.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,730.00
inventory 1g
10-20 days ฿35,440.00

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Methyl 6-bromo-2-methyl-1H-indole-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its structure supports the construction of complex indole-based molecules with biological activity. Commonly employed in medicinal chemistry for creating analogs in drug discovery programs targeting neurological disorders and inflammation. Also utilized in research settings to prepare fluorescent probes and labeled compounds for

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of serotonin receptor modulators and other central nervous system agents. Its structure supports the construction of complex indole-based molecules with biological activity. Commonly employed in medicinal chemistry for creating analogs in drug discovery programs targeting neurological disorders and inflammation. Also utilized in research settings to prepare fluorescent probes and labeled compounds for biochemical assays.

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