4'-Aminoacetophenone

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99%

Reagent Code: #134745
$product.alias - string(129) "p-aminoacetophenone; 4-aminoacetophenone, p-aminobenzylketone, p-a-acetylbenzene, p-aminoacetylbenzene, p-aminophenylmethylketone"
label
Alias p-aminoacetophenone; 4-aminoacetophenone, p-aminobenzylketone, p-a-acetylbenzene, p-aminoacetylbenzene, p-aminophenylmethylketone
product.cas - string(7) "99-92-3"
product.physical_n_chem_properties - string(0) ""
fingerprint
CAS Number 99-92-3

science Other reagents with same CAS 99-92-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.16 g/mol
Formula C₈H₉NO
badge Registry Numbers
EC Number 202-801-2
MDL Number MFCD00007896
thermostat Physical Properties
Melting Point 103-107 °C(lit.)
Boiling Point 293 °C(lit.)
inventory_2 Storage & Handling
Density 0.77 g/cm
Storage Room temperature, cool

description Product Description

Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It plays a role in the preparation of azo dyes and pigments due to its aromatic amine functionality. Also employed in the development of certain analgesics and anti-inflammatory agents. Its reactivity makes it valuable in forming Schiff bases and other nitrogen-containing compounds used in medicinal chemistry. Additionally, it finds use in research settings for synthesizing novel compounds with potential biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿550.00
inventory 100g
10-20 days ฿1,400.00
inventory 500g
10-20 days ฿5,200.00
inventory 2.5kg
10-20 days ฿21,450.00

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4'-Aminoacetophenone
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Used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and fine chemicals. It plays a role in the preparation of azo dyes and pigments due to its aromatic amine functionality. Also employed in the development of certain analgesics and anti-inflammatory agents. Its reactivity makes it valuable in forming Schiff bases and other nitrogen-containing compounds used in medicinal chemistry. Additionally, it finds use in research settings for synthesizing novel compounds with potential biological activity.
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