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

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Reagent Code: #132041
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CAS Number 37777-70-1

science Other reagents with same CAS 37777-70-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.59 g/mol
Formula C₈H₆ClNO₄
badge Registry Numbers
MDL Number MFCD01411947
thermostat Physical Properties
Melting Point 174-175 °C(Solv: acetic acid (64-19-7); water (7732-18-5))
Boiling Point 398.3±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.532±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs). It plays a key role in constructing complex organic molecules where a nitro-substituted aromatic system is required for further functionalization. The presence of both chloro and nitro groups allows for selective reactions, making it valuable in multi-step organic syntheses. Commonly employed in research settings for preparing biologically active compounds and in the production of specialty chemicals.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿960.00
inventory 1g
10-20 days ฿2,430.00
inventory 5g
10-20 days ฿9,850.00

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2-(2-Chloro-5-nitrophenyl)acetic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs). It plays a key role in constructing complex organic molecules where a nitro-substituted aromatic system is required for further functionalization. The presence of both chloro and nitro groups allows for selective reactions, making it valuable in multi-step organic syntheses. Commonly employed in research settings for preparing biologically active compounds and in

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs). It plays a key role in constructing complex organic molecules where a nitro-substituted aromatic system is required for further functionalization. The presence of both chloro and nitro groups allows for selective reactions, making it valuable in multi-step organic syntheses. Commonly employed in research settings for preparing biologically active compounds and in the production of specialty chemicals.

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