5-Bromobenzo[d][1,3]dioxol-4-amine

98%

Reagent Code: #155152
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CAS Number 401811-78-7

science Other reagents with same CAS 401811-78-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 2163 g/mol
Formula C₇H₆BrNO₂
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MDL Number MFCD09038123
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and psychoactive drugs. It serves as a building block in the preparation of substituted benzodioxoles, which are found in certain antidepressants, antipsychotics, and cognitive enhancers. Also employed in research settings for the creation of novel amine-containing heterocyclic compounds with potential biological activity. Its bromo group allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,930.00

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5-Bromobenzo[d][1,3]dioxol-4-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and psychoactive drugs. It serves as a building block in the preparation of substituted benzodioxoles, which are found in certain antidepressants, antipsychotics, and cognitive enhancers. Also employed in research settings for the creation of novel amine-containing heterocyclic compounds with potential biological activity. Its bromo group allows for further functionalization vi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and psychoactive drugs. It serves as a building block in the preparation of substituted benzodioxoles, which are found in certain antidepressants, antipsychotics, and cognitive enhancers. Also employed in research settings for the creation of novel amine-containing heterocyclic compounds with potential biological activity. Its bromo group allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry and drug discovery.

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