6-Nitro-2,3-dihydrobenzofuran-5-amine

97%

Reagent Code: #218111
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CAS Number 84594-78-5

science Other reagents with same CAS 84594-78-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.16 g/mol
Formula C₈H₈N₂O₃
badge Registry Numbers
MDL Number MFCD25967717
thermostat Physical Properties
Boiling Point 370.5±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antidepressants. Its structure supports the creation of bioactive molecules due to the presence of both amine and nitro functional groups, which can be further modified. Commonly employed in research settings for designing compounds with neurological activity. Also utilized in the preparation of dyes and fluorescent probes for biochemical labeling, thanks to its aromatic framework and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,720.00
inventory 5g
10-20 days ฿5,270.00
inventory 10g
10-20 days ฿8,470.00
inventory 25g
10-20 days ฿18,920.00
6-Nitro-2,3-dihydrobenzofuran-5-amine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antidepressants. Its structure supports the creation of bioactive molecules due to the presence of both amine and nitro functional groups, which can be further modified. Commonly employed in research settings for designing compounds with neurological activity. Also utilized in the preparation of dyes and fluorescent probes for biochemical labeling, thanks to its aromatic frame

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antidepressants. Its structure supports the creation of bioactive molecules due to the presence of both amine and nitro functional groups, which can be further modified. Commonly employed in research settings for designing compounds with neurological activity. Also utilized in the preparation of dyes and fluorescent probes for biochemical labeling, thanks to its aromatic framework and reactivity profile.

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