2'-Amino-5'-hydroxyacetophenone

95%

Reagent Code: #137524
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CAS Number 30954-71-3

science Other reagents with same CAS 30954-71-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.16 g/mol
Formula C₈H₉NO₂
badge Registry Numbers
MDL Number MFCD13193239
thermostat Physical Properties
Melting Point 157-161 °C
Boiling Point 359 °C
inventory_2 Storage & Handling
Density 1.242 g/cm3
Storage 2-8°C, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of analgesic and anti-inflammatory agents. It serves as a building block in organic reactions where both the amino and hydroxyl functional groups can be selectively modified. Commonly employed in the development of heterocyclic compounds, including benzoxazoles and other nitrogen-containing rings with biological activity. Also utilized in research settings for the preparation of dyes and fluorescent probes due to its reactive sites and aromatic structure.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿32,770.00

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2'-Amino-5'-hydroxyacetophenone
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of analgesic and anti-inflammatory agents. It serves as a building block in organic reactions where both the amino and hydroxyl functional groups can be selectively modified. Commonly employed in the development of heterocyclic compounds, including benzoxazoles and other nitrogen-containing rings with biological activity. Also utilized in research settings for the preparation of dyes and fluorescent probes due to

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of analgesic and anti-inflammatory agents. It serves as a building block in organic reactions where both the amino and hydroxyl functional groups can be selectively modified. Commonly employed in the development of heterocyclic compounds, including benzoxazoles and other nitrogen-containing rings with biological activity. Also utilized in research settings for the preparation of dyes and fluorescent probes due to its reactive sites and aromatic structure.

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