Methyl 4-(4-methoxyphenyl)-3-oxobutanoate

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Reagent Code: #203135
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CAS Number 100117-84-8

science Other reagents with same CAS 100117-84-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.240 g/mol
Formula C₁₂H₁₄O₄
badge Registry Numbers
MDL Number MFCD08457127
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and related analgesic compounds. Its structure allows for easy functionalization, making it valuable in building complex molecules through condensation and cyclization reactions. Also employed in the preparation of heterocyclic compounds used in medicinal chemistry and agrochemical research. Its keto-ester functionality supports versatile reactivity, useful in both academic and industrial synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,200.00
inventory 250mg
10-20 days ฿8,800.00
inventory 1g
10-20 days ฿23,880.00

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Methyl 4-(4-methoxyphenyl)-3-oxobutanoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and related analgesic compounds. Its structure allows for easy functionalization, making it valuable in building complex molecules through condensation and cyclization reactions. Also employed in the preparation of heterocyclic compounds used in medicinal chemistry and agrochemical research. Its keto-ester functionality supports versatile reactivity, useful in b

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and related analgesic compounds. Its structure allows for easy functionalization, making it valuable in building complex molecules through condensation and cyclization reactions. Also employed in the preparation of heterocyclic compounds used in medicinal chemistry and agrochemical research. Its keto-ester functionality supports versatile reactivity, useful in both academic and industrial synthetic pathways.

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