6-Methyl isatoic anhydride

95%

Reagent Code: #207602
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CAS Number 4692-99-3

science Other reagents with same CAS 4692-99-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.16 g/mol
Formula C₉H₇NO₃
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. It serves as a building block in medicinal chemistry due to its ability to form amide and imide bonds, enabling the construction of heterocyclic frameworks common in drug molecules. Commonly employed in research settings for the preparation of fluorescent probes and labeling reagents owing to its reactive anhydride group. Also utilized in the development of agrochemicals and functional materials where aromatic scaffolds with defined substitution patterns are required.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,790.00
inventory 10g
10-20 days ฿5,520.00
inventory 25g
10-20 days ฿11,050.00
inventory 100g
10-20 days ฿29,080.00
6-Methyl isatoic anhydride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. It serves as a building block in medicinal chemistry due to its ability to form amide and imide bonds, enabling the construction of heterocyclic frameworks common in drug molecules. Commonly employed in research settings for the preparation of fluorescent probes and labeling reagents owing to its reactive anhydride group. Also utilized in the develo

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. It serves as a building block in medicinal chemistry due to its ability to form amide and imide bonds, enabling the construction of heterocyclic frameworks common in drug molecules. Commonly employed in research settings for the preparation of fluorescent probes and labeling reagents owing to its reactive anhydride group. Also utilized in the development of agrochemicals and functional materials where aromatic scaffolds with defined substitution patterns are required.

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