6-Isopropyl indole

97%

Reagent Code: #200391
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CAS Number 32996-24-0

science Other reagents with same CAS 32996-24-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 159.23 g/mol
Formula C₁₁H₁₃N
badge Registry Numbers
MDL Number MFCD07369790
thermostat Physical Properties
Melting Point 36-40 °C(lit.)
Boiling Point 281.3±9.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.047±0.06 g/cm3(Predicted)
Storage Room temperature, dry, sealed

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of serotonin receptor modulators. It serves as a building block in creating compounds with potential neurological and psychiatric applications, including antidepressants and anti-anxiety agents. Also explored in the design of kinase inhibitors for cancer research due to its structural similarity to bioactive indole derivatives. Its lipophilic isopropyl group enhances membrane permeability, improving cellular uptake in drug candidates.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿12,920.00
inventory 5g
10-20 days ฿45,240.00

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6-Isopropyl indole
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of serotonin receptor modulators. It serves as a building block in creating compounds with potential neurological and psychiatric applications, including antidepressants and anti-anxiety agents. Also explored in the design of kinase inhibitors for cancer research due to its structural similarity to bioactive indole derivatives. Its lipophilic isopropyl group enhances membrane permeability, improving cellular uptake in dru
Used in the synthesis of pharmaceutical intermediates, particularly in the development of serotonin receptor modulators. It serves as a building block in creating compounds with potential neurological and psychiatric applications, including antidepressants and anti-anxiety agents. Also explored in the design of kinase inhibitors for cancer research due to its structural similarity to bioactive indole derivatives. Its lipophilic isopropyl group enhances membrane permeability, improving cellular uptake in drug candidates.
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