(3-Iodophenyl)methanesulfonyl chloride

95%

Reagent Code: #201247
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CAS Number 352708-55-5

science Other reagents with same CAS 352708-55-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.54 g/mol
Formula C₇H₆ClIO₂S
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MDL Number MFCD22373777
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of radiolabeled agents for medical imaging. Its structure allows for easy incorporation of iodine-123 or iodine-131, making it valuable in creating tracers for single-photon emission computed tomography (SPECT). It is also employed in the preparation of sulfonamide-based bioactive molecules, where the sulfonyl chloride group reacts selectively with amines to form stable sulfonamide bonds. Due to its reactivity, it facilitates the construction of complex organic molecules in medicinal chemistry research, especially in CNS-targeted drug discovery and oncology-related compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿22,210.00
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(3-Iodophenyl)methanesulfonyl chloride
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Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of radiolabeled agents for medical imaging. Its structure allows for easy incorporation of iodine-123 or iodine-131, making it valuable in creating tracers for single-photon emission computed tomography (SPECT). It is also employed in the preparation of sulfonamide-based bioactive molecules, where the sulfonyl chloride group reacts selectively with amines to form stable sulfonamide bonds. Du

Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of radiolabeled agents for medical imaging. Its structure allows for easy incorporation of iodine-123 or iodine-131, making it valuable in creating tracers for single-photon emission computed tomography (SPECT). It is also employed in the preparation of sulfonamide-based bioactive molecules, where the sulfonyl chloride group reacts selectively with amines to form stable sulfonamide bonds. Due to its reactivity, it facilitates the construction of complex organic molecules in medicinal chemistry research, especially in CNS-targeted drug discovery and oncology-related compounds.

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