4-Hydroxyisobenzofuran-1(3H)-one

95%

Reagent Code: #196319
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CAS Number 13161-32-5

science Other reagents with same CAS 13161-32-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.13 g/mol
Formula C₈H₆O₃
badge Registry Numbers
MDL Number MFCD15143974
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Widely used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anticoagulant drugs. It serves as a key building block in the preparation of warfarin and related coumarin derivatives due to its structural similarity to the core scaffold of these compounds. Its lactone functionality allows for selective chemical modifications, making it valuable in medicinal chemistry for creating bioactive molecules. Additionally, it is employed in the synthesis of fluorescent dyes and optical brighteners used in textiles and paper industries. Its reactivity and stability under various reaction conditions enhance its utility in organic synthesis and industrial applications.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿5,990.00
inventory 100mg
10-20 days ฿14,990.00
inventory 250mg
10-20 days ฿33,960.00

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4-Hydroxyisobenzofuran-1(3H)-one
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Widely used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anticoagulant drugs. It serves as a key building block in the preparation of warfarin and related coumarin derivatives due to its structural similarity to the core scaffold of these compounds. Its lactone functionality allows for selective chemical modifications, making it valuable in medicinal chemistry for creating bioactive molecules. Additionally, it is employed in the synthesis of fluorescent dyes

Widely used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anticoagulant drugs. It serves as a key building block in the preparation of warfarin and related coumarin derivatives due to its structural similarity to the core scaffold of these compounds. Its lactone functionality allows for selective chemical modifications, making it valuable in medicinal chemistry for creating bioactive molecules. Additionally, it is employed in the synthesis of fluorescent dyes and optical brighteners used in textiles and paper industries. Its reactivity and stability under various reaction conditions enhance its utility in organic synthesis and industrial applications.

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