2-(5-Chloro-2-nitrophenyl)acetic acid

≥95%

Reagent Code: #162209
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CAS Number 22908-28-7

science Other reagents with same CAS 22908-28-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.59 g/mol
Formula C₈H₆ClNO₄
badge Registry Numbers
MDL Number MFCD03206465
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

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 introducing substituted phenylacetic acid moieties, which are common in drug molecules targeting pain and inflammation. Also employed in organic synthesis for constructing more complex nitroaromatic compounds. Its nitro and chloro functional groups allow for further chemical modifications, such as reductions and nucleophilic substitutions, making it valuable in medicinal chemistry research.

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Test Parameter Specification
Appearance Solid
Purity (%) 95-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,360.00
inventory 250mg
10-20 days ฿14,730.00

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2-(5-Chloro-2-nitrophenyl)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 introducing substituted phenylacetic acid moieties, which are common in drug molecules targeting pain and inflammation. Also employed in organic synthesis for constructing more complex nitroaromatic compounds. Its nitro and chloro functional groups allow for further chemical modifications, such as reductions and nucleophilic subst

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 introducing substituted phenylacetic acid moieties, which are common in drug molecules targeting pain and inflammation. Also employed in organic synthesis for constructing more complex nitroaromatic compounds. Its nitro and chloro functional groups allow for further chemical modifications, such as reductions and nucleophilic substitutions, making it valuable in medicinal chemistry research.

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