methyl 3-iodo-1-(phenylsulfonyl)-1H-indole-2-carboxylate

≥90%

Reagent Code: #197443
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CAS Number 860611-94-5

science Other reagents with same CAS 860611-94-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 441.24 g/mol
Formula C₁₆H₁₂INO₄S
badge Registry Numbers
MDL Number MFCD04124189
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active indole derivatives, particularly in pharmaceutical research. Its structure allows for selective functionalization at multiple sites, making it valuable in the development of kinase inhibitors and anti-inflammatory agents. The presence of the iodo group enables cross-coupling reactions such as Suzuki or Heck reactions, facilitating the construction of complex molecular architectures. Additionally, the sulfonyl and ester groups act as directing or protecting groups during synthesis, enhancing regio- and stereocontrol. Commonly employed in medicinal chemistry for generating compound libraries aimed at targeting central nervous system disorders and cancer-related pathways.

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Test Parameter Specification
Appearance Solid
Purity (%) 90-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿6,640.00

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methyl 3-iodo-1-(phenylsulfonyl)-1H-indole-2-carboxylate
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Used as a key intermediate in the synthesis of biologically active indole derivatives, particularly in pharmaceutical research. Its structure allows for selective functionalization at multiple sites, making it valuable in the development of kinase inhibitors and anti-inflammatory agents. The presence of the iodo group enables cross-coupling reactions such as Suzuki or Heck reactions, facilitating the construction of complex molecular architectures. Additionally, the sulfonyl and ester groups act as directing or protecting groups during synthesis, enhancing regio- and stereocontrol. Commonly employed in medicinal chemistry for generating compound libraries aimed at targeting central nervous system disorders and cancer-related pathways.
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