4'-Aminoacetophenone

Reagent grade, 98%

Reagent Code: #134744
label
Alias p-aminoacetophenone; 4-aminoacetophenone, p-aminobenzylketone, p-a-acetylbenzene, p-aminoacetylbenzene, p-aminophenylmethylketone
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 the synthesis of pharmaceuticals, particularly in the production of analgesics and anti-inflammatory drugs. It serves as a building block in organic synthesis for creating more complex molecules due to the presence of both amine and ketone functional groups. Also employed in the development of dyes and pigments, and occasionally in the preparation of agrochemicals. Its reactivity makes it valuable in forming Schiff bases and other derivatives used in medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿300.00
inventory 50g
10-20 days ฿690.00
inventory 250g
10-20 days ฿2,250.00
inventory 1kg
10-20 days ฿8,860.00
4'-Aminoacetophenone
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of analgesics and anti-inflammatory drugs. It serves as a building block in organic synthesis for creating more complex molecules due to the presence of both amine and ketone functional groups. Also employed in the development of dyes and pigments, and occasionally in the preparation of agrochemicals. Its reactivity makes it valuable in forming Schiff bases and other derivatives used in medicinal chemistry research.
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of analgesics and anti-inflammatory drugs. It serves as a building block in organic synthesis for creating more complex molecules due to the presence of both amine and ketone functional groups. Also employed in the development of dyes and pigments, and occasionally in the preparation of agrochemicals. Its reactivity makes it valuable in forming Schiff bases and other derivatives used in medicinal chemistry research.
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