2-(3,5-Dichloro-2-hydroxyphenyl)acetic acid

95%

Reagent Code: #178613
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CAS Number 38692-69-2

science Other reagents with same CAS 38692-69-2

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Weight 221.04 g/mol
Formula C₈H₆Cl₂O₃
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block for arylacetic acid derivatives, which exhibit analgesic and antipyretic properties. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing compounds with improved biological activity and selectivity. Also employed in research settings for designing enzyme inhibitors and studying structure-activity relationships in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,200.00
inventory 1g
10-20 days ฿22,010.00
inventory 250mg
10-20 days ฿6,820.00

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2-(3,5-Dichloro-2-hydroxyphenyl)acetic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block for arylacetic acid derivatives, which exhibit analgesic and antipyretic properties. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing compounds with improved biological activity and selectivity. Also employed in research settings for designing enzyme inhibitors and studying stru

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs). It serves as a building block for arylacetic acid derivatives, which exhibit analgesic and antipyretic properties. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing compounds with improved biological activity and selectivity. Also employed in research settings for designing enzyme inhibitors and studying structure-activity relationships in drug candidates.

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