2,2',4'-Trichloroacetophenone

98.0%

Reagent Code: #239988
label
Alias 2,4-Dichlorobenzoylmethylchloride; Trichloroacetophenone
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CAS Number 4252-78-2

science Other reagents with same CAS 4252-78-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.48 g/mol
Formula C₈H₅Cl₃O
badge Registry Numbers
MDL Number MFCD00000934
thermostat Physical Properties
Melting Point 47-54 °C(lit.)
Boiling Point 130-135 °C4 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.312 g/cm3
Storage Room temperature

description Product Description

Used primarily as a chemical intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of certain antihistamines and nonsteroidal anti-inflammatory drugs (NSAIDs) due to its reactive carbonyl and chlorinated aromatic structure. Also employed in the preparation of specialty chemicals, including UV absorbers and dyes. Its electrophilic nature makes it valuable in organic transformations such as Friedel-Crafts acylation and nucleophilic substitution reactions. Handle with care due to potential irritant properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿280.00
inventory 25g
10-20 days ฿340.00
inventory 100g
10-20 days ฿660.00
inventory 500g
10-20 days ฿2,980.00
inventory 2.5kg
10-20 days ฿13,350.00

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2,2',4'-Trichloroacetophenone
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Used primarily as a chemical intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of certain antihistamines and nonsteroidal anti-inflammatory drugs (NSAIDs) due to its reactive carbonyl and chlorinated aromatic structure. Also employed in the preparation of specialty chemicals, including UV absorbers and dyes. Its electrophilic nature makes it valuable in organic transformations such as Friedel-Crafts acylation and nucleophilic substitution reactions.

Used primarily as a chemical intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of certain antihistamines and nonsteroidal anti-inflammatory drugs (NSAIDs) due to its reactive carbonyl and chlorinated aromatic structure. Also employed in the preparation of specialty chemicals, including UV absorbers and dyes. Its electrophilic nature makes it valuable in organic transformations such as Friedel-Crafts acylation and nucleophilic substitution reactions. Handle with care due to potential irritant properties.

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