4-(2-Chlorophenyl)-4-oxobutanoic acid

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Reagent Code: #46152
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CAS Number 106263-50-7

science Other reagents with same CAS 106263-50-7

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Weight 212.6297 g/mol
Formula C₁₀H₉ClO₃
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MDL Number MFCD03844205
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4-(2-Chlorophenyl)-4-oxobutanoic acid is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring both a chlorophenyl group and a carboxylic acid moiety, makes it a versatile building block for the development of drugs, particularly those targeting neurological and inflammatory conditions. It is often employed in the synthesis of benzodiazepine derivatives, which are widely used as anxiolytics, sedatives, and muscle relaxants. Additionally, its reactive carbonyl group allows for further chemical modifications, enabling the creation of diverse molecules with potential therapeutic applications. In research, it serves as a precursor for studying structure-activity relationships in drug design, aiding in the discovery of new bioactive compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,007.00
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4-(2-Chlorophenyl)-4-oxobutanoic acid
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4-(2-Chlorophenyl)-4-oxobutanoic acid is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring both a chlorophenyl group and a carboxylic acid moiety, makes it a versatile building block for the development of drugs, particularly those targeting neurological and inflammatory conditions. It is often employed in the synthesis of benzodiazepine derivatives, which are widely used as anxiolytics, sedatives, and muscle rela

4-(2-Chlorophenyl)-4-oxobutanoic acid is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceutical compounds. Its structure, featuring both a chlorophenyl group and a carboxylic acid moiety, makes it a versatile building block for the development of drugs, particularly those targeting neurological and inflammatory conditions. It is often employed in the synthesis of benzodiazepine derivatives, which are widely used as anxiolytics, sedatives, and muscle relaxants. Additionally, its reactive carbonyl group allows for further chemical modifications, enabling the creation of diverse molecules with potential therapeutic applications. In research, it serves as a precursor for studying structure-activity relationships in drug design, aiding in the discovery of new bioactive compounds.

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