3-(4-Methylbenzoyl)propionic acid

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Reagent Code: #206109
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CAS Number 4619-20-9

science Other reagents with same CAS 4619-20-9

blur_circular Chemical Specifications

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Weight 192.21 g/mol
Formula C₁₁H₁₂O₃
badge Registry Numbers
MDL Number MFCD00020541
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceuticals and fine chemicals, particularly as an intermediate in the production of nonsteroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic synthesis due to its reactive carbonyl and carboxylic acid functional groups, enabling esterification, reduction, and condensation reactions. Also employed in the development of photoinitiators for UV-curable coatings and resins, where it contributes to efficient radical generation upon light exposure. Its aromatic ketone structure makes it useful in designing compounds for specialty polymers and agrochemicals.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿410.00
inventory 25g
10-20 days ฿1,810.00
inventory 100g
10-20 days ฿6,340.00

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3-(4-Methylbenzoyl)propionic acid
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Used in the synthesis of pharmaceuticals and fine chemicals, particularly as an intermediate in the production of nonsteroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic synthesis due to its reactive carbonyl and carboxylic acid functional groups, enabling esterification, reduction, and condensation reactions. Also employed in the development of photoinitiators for UV-curable coatings and resins, where it contributes to efficient radical generation upon light exposure. Its

Used in the synthesis of pharmaceuticals and fine chemicals, particularly as an intermediate in the production of nonsteroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic synthesis due to its reactive carbonyl and carboxylic acid functional groups, enabling esterification, reduction, and condensation reactions. Also employed in the development of photoinitiators for UV-curable coatings and resins, where it contributes to efficient radical generation upon light exposure. Its aromatic ketone structure makes it useful in designing compounds for specialty polymers and agrochemicals.

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