trans-3-(4-Chlorobenzoyl)acrylic acid

97%

Reagent Code: #159106
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CAS Number 29582-39-6

science Other reagents with same CAS 29582-39-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.61 g/mol
Formula ClC₆H₄COCH=CHCO₂H
badge Registry Numbers
MDL Number MFCD00041465
inventory_2 Storage & Handling
Storage 2~8 ℃

description Product Description

Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of benzophenone-based pharmaceuticals. It serves as a building block for compounds exhibiting anti-inflammatory, analgesic, and antipyretic activities. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing drug candidates. Also employed in the preparation of photoinitiators used in UV-curable coatings and resins due to its conjugated carbonyl system that responds well to UV light.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿550.00
inventory 5g
10-20 days ฿1,940.00
inventory 25g
10-20 days ฿8,620.00
inventory 100g
10-20 days ฿32,840.00

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trans-3-(4-Chlorobenzoyl)acrylic acid
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Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of benzophenone-based pharmaceuticals. It serves as a building block for compounds exhibiting anti-inflammatory, analgesic, and antipyretic activities. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing drug candidates. Also employed in the preparation of photoinitiators used in UV-curable coatings and resins due to its conjug

Used as a key intermediate in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), particularly in the production of benzophenone-based pharmaceuticals. It serves as a building block for compounds exhibiting anti-inflammatory, analgesic, and antipyretic activities. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing drug candidates. Also employed in the preparation of photoinitiators used in UV-curable coatings and resins due to its conjugated carbonyl system that responds well to UV light.

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