4-Chloro-2-methoxybenzoic acid

98%

Reagent Code: #159553
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Alias 2-methoxy-4-chlorobenzoic acid
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CAS Number 57479-70-6

science Other reagents with same CAS 57479-70-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.59 g/mol
Formula C₈H₇ClO₃
badge Registry Numbers
MDL Number MFCD00002532
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of selective herbicides and plant growth regulators. Its structure allows for modification in active compounds targeting specific enzymatic pathways in plants. Also employed in research for developing new derivatives with biological activity, including antimicrobial and anti-inflammatory agents. The presence of both chloro and methoxy functional groups enhances its reactivity in coupling reactions and heterocycle formation.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,150.00
inventory 100g
10-20 days ฿4,560.00
inventory 500g
10-20 days ฿21,350.00

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4-Chloro-2-methoxybenzoic acid
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of selective herbicides and plant growth regulators. Its structure allows for modification in active compounds targeting specific enzymatic pathways in plants. Also employed in research for developing new derivatives with biological activity, including antimicrobial and anti-inflammatory agents. The presence of both chloro and methoxy functional groups enhances its reactivity in coupling reaction

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of selective herbicides and plant growth regulators. Its structure allows for modification in active compounds targeting specific enzymatic pathways in plants. Also employed in research for developing new derivatives with biological activity, including antimicrobial and anti-inflammatory agents. The presence of both chloro and methoxy functional groups enhances its reactivity in coupling reactions and heterocycle formation.

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