1-Bromo-2,5-dimethoxy-4-((4-methoxybenzyl)oxy)benzene

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Reagent Code: #146106
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CAS Number 1646152-54-6

science Other reagents with same CAS 1646152-54-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 353.21 g/mol
Formula C₁₆H₁₇BrO₄
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of psychoactive compounds, particularly in the production of substituted phenethylamines and analogs related to the 2C family of hallucinogens. Its primary application is in research settings for exploring structure-activity relationships in neurochemical studies. The compound enables selective modifications in aromatic ring systems, making it valuable for creating derivatives with potential affinity for serotonin receptors. Due to its role in synthesizing controlled substance analogs, it is mainly restricted to forensic and pharmaceutical research under regulated conditions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿790.00
inventory 1g
10-20 days ฿2,260.00

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1-Bromo-2,5-dimethoxy-4-((4-methoxybenzyl)oxy)benzene
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Used as an intermediate in the synthesis of psychoactive compounds, particularly in the production of substituted phenethylamines and analogs related to the 2C family of hallucinogens. Its primary application is in research settings for exploring structure-activity relationships in neurochemical studies. The compound enables selective modifications in aromatic ring systems, making it valuable for creating derivatives with potential affinity for serotonin receptors. Due to its role in synthesizing control

Used as an intermediate in the synthesis of psychoactive compounds, particularly in the production of substituted phenethylamines and analogs related to the 2C family of hallucinogens. Its primary application is in research settings for exploring structure-activity relationships in neurochemical studies. The compound enables selective modifications in aromatic ring systems, making it valuable for creating derivatives with potential affinity for serotonin receptors. Due to its role in synthesizing controlled substance analogs, it is mainly restricted to forensic and pharmaceutical research under regulated conditions.

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