(5-Iodo-2-methylphenyl)(5-phenylthiophen-2-yl)methanone

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Reagent Code: #201196
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CAS Number 2070015-44-8

science Other reagents with same CAS 2070015-44-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 404.26 g/mol
Formula C₁₈H₁₃IOS
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Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports cross-coupling reactions, making it valuable in developing drug candidates for cancer and inflammatory diseases. The iodo substituent allows for further functionalization via palladium-catalyzed reactions, while the thiophene and phenyl groups contribute to binding selectivity in receptor sites. Commonly employed in medicinal chemistry for building complex aromatic frameworks with enhanced metabolic stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10mg
10-20 days ฿62,670.00
(5-Iodo-2-methylphenyl)(5-phenylthiophen-2-yl)methanone
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports cross-coupling reactions, making it valuable in developing drug candidates for cancer and inflammatory diseases. The iodo substituent allows for further functionalization via palladium-catalyzed reactions, while the thiophene and phenyl groups contribute to binding selectivity in receptor sites. Commonly employed in medicinal chemistry f

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure supports cross-coupling reactions, making it valuable in developing drug candidates for cancer and inflammatory diseases. The iodo substituent allows for further functionalization via palladium-catalyzed reactions, while the thiophene and phenyl groups contribute to binding selectivity in receptor sites. Commonly employed in medicinal chemistry for building complex aromatic frameworks with enhanced metabolic stability.

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