4-(4-Methylbenzoyl)-1H-pyrrole-2-carboxylic acid

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Reagent Code: #46331
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CAS Number 886361-19-9

science Other reagents with same CAS 886361-19-9

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Weight 229.2300 g/mol
Formula C₁₃H₁₁NO₃
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MDL Number MFCD05663824
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both a pyrrole ring and a 4-methylbenzoyl group, makes it particularly valuable in the development of molecules with potential therapeutic effects. Researchers often employ it in the synthesis of novel drug candidates, especially those targeting inflammation, cancer, or neurological disorders. Additionally, its carboxylic acid group allows for further functionalization, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. This compound is also explored in material science for the development of organic semiconductors or light-emitting materials due to its conjugated system.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,907.00

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4-(4-Methylbenzoyl)-1H-pyrrole-2-carboxylic acid
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both a pyrrole ring and a 4-methylbenzoyl group, makes it particularly valuable in the development of molecules with potential therapeutic effects. Researchers often employ it in the synthesis of novel drug candidates, especially those targeting inflammation, cancer, or neurological disorders. Additionally, i

This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both a pyrrole ring and a 4-methylbenzoyl group, makes it particularly valuable in the development of molecules with potential therapeutic effects. Researchers often employ it in the synthesis of novel drug candidates, especially those targeting inflammation, cancer, or neurological disorders. Additionally, its carboxylic acid group allows for further functionalization, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. This compound is also explored in material science for the development of organic semiconductors or light-emitting materials due to its conjugated system.

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