2-methyl-2-(4-nitrophenyl)propanoic acid

95%

Reagent Code: #209296
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CAS Number 42206-47-3

science Other reagents with same CAS 42206-47-3

blur_circular Chemical Specifications

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Weight 209.07 g/mol
Formula C₁₀H₁₁NO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its nitro group allows for further functionalization, such as reduction to an amine, enabling the construction of more complex molecules. Commonly employed in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and related derivatives due to its structural similarity to known bioactive compounds. Also utilized in research settings for studying reaction mechanisms involving aromatic nitro compounds and carboxylic acid derivatives.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿242.00
inventory 250mg
10-20 days ฿429.00
inventory 1g
10-20 days ฿1,340.00
inventory 5g
10-20 days ฿4,580.00

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2-methyl-2-(4-nitrophenyl)propanoic acid
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its nitro group allows for further functionalization, such as reduction to an amine, enabling the construction of more complex molecules. Commonly employed in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and related derivatives due to its structural similarity to known bioactive compounds. Also utilized in research settings for studying reaction mechanisms involving aroma
Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its nitro group allows for further functionalization, such as reduction to an amine, enabling the construction of more complex molecules. Commonly employed in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and related derivatives due to its structural similarity to known bioactive compounds. Also utilized in research settings for studying reaction mechanisms involving aromatic nitro compounds and carboxylic acid derivatives.
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