Methyl 4-chloro-3-hydroxy-5-nitrobenzoate

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Reagent Code: #128863
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CAS Number 180031-12-3

science Other reagents with same CAS 180031-12-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.59 g/mol
Formula C₈H₆ClNO₅
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MDL Number MFCD28397262
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—chloro, hydroxy, and nitro—allow for selective chemical modifications, making it valuable in constructing complex organic compounds. Commonly employed in research settings for derivatization reactions and in the preparation of ester and amide analogs for drug discovery. Also utilized in the development of agrochemicals due to its reactivity and structural features that support the design of novel active ingredients.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,140.00
inventory 250mg
10-20 days ฿6,920.00
inventory 1g
10-20 days ฿13,480.00

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Methyl 4-chloro-3-hydroxy-5-nitrobenzoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—chloro, hydroxy, and nitro—allow for selective chemical modifications, making it valuable in constructing complex organic compounds. Commonly employed in research settings for derivatization reactions and in the preparation of ester and amide analogs for drug discovery. Also utilized in the development of agroch

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its functional groups—chloro, hydroxy, and nitro—allow for selective chemical modifications, making it valuable in constructing complex organic compounds. Commonly employed in research settings for derivatization reactions and in the preparation of ester and amide analogs for drug discovery. Also utilized in the development of agrochemicals due to its reactivity and structural features that support the design of novel active ingredients.

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