4-Benzoyl-5-methyldihydrofuran-2(3H)-one

≥95%

Reagent Code: #148730
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CAS Number 101563-78-4

science Other reagents with same CAS 101563-78-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.22 g/mol
Formula C₁₂H₁₂O₃
badge Registry Numbers
MDL Number MFCD28348658
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports the formation of bioactive molecules due to the presence of reactive functional groups. Commonly employed in organic synthesis for constructing complex lactone frameworks. Also utilized in the preparation of photoinitiators for polymer chemistry, where it contributes to UV-curable resin systems. Shows utility in agrochemical formulations for enhancing stability and reactivity of active ingredients.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿39,900.00
5g
10-20 days ฿79,800.00

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4-Benzoyl-5-methyldihydrofuran-2(3H)-one
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports the formation of bioactive molecules due to the presence of reactive functional groups. Commonly employed in organic synthesis for constructing complex lactone frameworks. Also utilized in the preparation of photoinitiators for polymer chemistry, where it contributes to UV-curable resin systems. Shows utility in agrochemical formulations for enh

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports the formation of bioactive molecules due to the presence of reactive functional groups. Commonly employed in organic synthesis for constructing complex lactone frameworks. Also utilized in the preparation of photoinitiators for polymer chemistry, where it contributes to UV-curable resin systems. Shows utility in agrochemical formulations for enhancing stability and reactivity of active ingredients.

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