6-Iodo-1H-3,1-benzoxazine-2,4-dione

97%

Reagent Code: #200632
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CAS Number 116027-10-2

science Other reagents with same CAS 116027-10-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.03 g/mol
Formula C₈H₄INO₃
badge Registry Numbers
MDL Number MFCD06661932
inventory_2 Storage & Handling
Storage 2-8°C, light-proof storage, inert atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of heterocyclic molecules with potential biological activity. Its iodo-substituted benzoxazine structure allows for further functionalization through reactions such as nucleophilic substitutions and transition metal-catalyzed cross-coupling processes, making it valuable in medicinal chemistry research for creating novel drug candidates and complex organic frameworks. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays due to the iodine moiety, which can serve as a radiolabel or aid in detection.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿740.00
inventory 250mg
10-20 days ฿1,290.00
inventory 1g
10-20 days ฿2,980.00
inventory 5g
10-20 days ฿8,500.00
6-Iodo-1H-3,1-benzoxazine-2,4-dione
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of heterocyclic molecules with potential biological activity. Its iodo-substituted benzoxazine structure allows for further functionalization through reactions such as nucleophilic substitutions and transition metal-catalyzed cross-coupling processes, making it valuable in medicinal chemistry research for creating novel drug candidates and complex organic frameworks. Also utilized in the preparation of f

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of heterocyclic molecules with potential biological activity. Its iodo-substituted benzoxazine structure allows for further functionalization through reactions such as nucleophilic substitutions and transition metal-catalyzed cross-coupling processes, making it valuable in medicinal chemistry research for creating novel drug candidates and complex organic frameworks. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays due to the iodine moiety, which can serve as a radiolabel or aid in detection.

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