Methyl 1-oxo-1,3-dihydroisobenzofuran-5-carboxylate

≥95%

Reagent Code: #208709
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CAS Number 23405-32-5

science Other reagents with same CAS 23405-32-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.17 g/mol
Formula C₁₀H₈O₄
badge Registry Numbers
MDL Number MFCD11046461
thermostat Physical Properties
Boiling Point 399.127°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of biologically active compounds targeting central nervous system disorders. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building complex lactone-based molecules. It is also employed in the development of agrochemicals and specialty polymers due to its reactive carbonyl and ester groups, which facilitate coupling and ring-opening reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,100.00
inventory 10g
10-20 days ฿3,220.00
inventory 25g
10-20 days ฿8,040.00

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Methyl 1-oxo-1,3-dihydroisobenzofuran-5-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of biologically active compounds targeting central nervous system disorders. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building complex lactone-based molecules. It is also employed in the development of agrochemicals and specialty polymers due to its reactive carbonyl and ester groups, which facilitate coupling and ring-opening reactions.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of biologically active compounds targeting central nervous system disorders. Its structure allows for functionalization at multiple sites, making it valuable in medicinal chemistry for building complex lactone-based molecules. It is also employed in the development of agrochemicals and specialty polymers due to its reactive carbonyl and ester groups, which facilitate coupling and ring-opening reactions.

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