N-(2-Iodophenyl)acetamide

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Reagent Code: #218828
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CAS Number 19591-17-4

science Other reagents with same CAS 19591-17-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.06 g/mol
Formula C₈H₈INO
badge Registry Numbers
MDL Number MFCD00099251
thermostat Physical Properties
Boiling Point 362.7 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. It serves as a building block in the development of bioactive molecules due to the presence of both an amide and an iodine substituent, which can undergo various transformations such as cross-coupling reactions. Commonly employed in the synthesis of indoles and related structures through intramolecular cyclization processes. Also utilized in medicinal chemistry for the design of potential drug candidates targeting neurological and inflammatory conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,890.00
inventory 1g
10-20 days ฿5,390.00
inventory 250mg
10-20 days ฿2,340.00

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N-(2-Iodophenyl)acetamide
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Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. It serves as a building block in the development of bioactive molecules due to the presence of both an amide and an iodine substituent, which can undergo various transformations such as cross-coupling reactions. Commonly employed in the synthesis of indoles and related structures through intramolecular cyclization processes. Also utilized in medicinal chemistry for the design of po

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. It serves as a building block in the development of bioactive molecules due to the presence of both an amide and an iodine substituent, which can undergo various transformations such as cross-coupling reactions. Commonly employed in the synthesis of indoles and related structures through intramolecular cyclization processes. Also utilized in medicinal chemistry for the design of potential drug candidates targeting neurological and inflammatory conditions.

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