7-Iodo-2H-1,4-benzoxazin-3(4H)-one

95%

Reagent Code: #199558
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CAS Number 874840-87-6

science Other reagents with same CAS 874840-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.04 g/mol
Formula C₈H₆INO₂
badge Registry Numbers
MDL Number MFCD07774202
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents and antipsychotic drugs. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating analogs with improved bioavailability and receptor binding. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or heteroaryl groups at the 7-position, enabling the exploration of structure-activity relationships in drug discovery programs. Also utilized in radiolabeling studies due to the presence of iodine, facilitating imaging and metabolic tracking.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,240.00
250mg
10-20 days ฿8,880.00
1g
10-20 days ฿23,930.00
7-Iodo-2H-1,4-benzoxazin-3(4H)-one
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents and antipsychotic drugs. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating analogs with improved bioavailability and receptor binding. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or heteroaryl groups at the 7-position, enabling the exploration of structure-activ

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents and antipsychotic drugs. Its structure allows for selective modification, making it valuable in medicinal chemistry for creating analogs with improved bioavailability and receptor binding. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or heteroaryl groups at the 7-position, enabling the exploration of structure-activity relationships in drug discovery programs. Also utilized in radiolabeling studies due to the presence of iodine, facilitating imaging and metabolic tracking.

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