2,4-Dimethylphenylacetic Acid

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Reagent Code: #172762
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CAS Number 6331-04-0

science Other reagents with same CAS 6331-04-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.20 g/mol
Formula C₁₀H₁₂O₂
badge Registry Numbers
MDL Number MFCD02664685
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the production of non-steroidal anti-inflammatory drugs (NSAIDs) due to its structural similarity to other arylacetic acid derivatives known for analgesic and anti-inflammatory properties. Also employed in the development of crop protection agents, where it acts as a building block for herbicides and plant growth regulators. Its substituted aromatic ring enhances lipophilicity, improving cell membrane penetration in biologically active molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿660.00

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2,4-Dimethylphenylacetic Acid
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the production of non-steroidal anti-inflammatory drugs (NSAIDs) due to its structural similarity to other arylacetic acid derivatives known for analgesic and anti-inflammatory properties. Also employed in the development of crop protection agents, where it acts as a building block for herbicides and plant growth regulators. Its substituted aromatic ring enhances lipophilicity, improving cell membrane penet
Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the production of non-steroidal anti-inflammatory drugs (NSAIDs) due to its structural similarity to other arylacetic acid derivatives known for analgesic and anti-inflammatory properties. Also employed in the development of crop protection agents, where it acts as a building block for herbicides and plant growth regulators. Its substituted aromatic ring enhances lipophilicity, improving cell membrane penetration in biologically active molecules.
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