3-Chloro-5-methoxybenzoic acid

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Reagent Code: #159011
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CAS Number 82477-67-6

science Other reagents with same CAS 82477-67-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.59 g/mol
Formula C₈H₇ClO₃
badge Registry Numbers
MDL Number MFCD01317994
thermostat Physical Properties
Melting Point 172-176 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It serves as a building block in agrochemicals for developing herbicides and plant growth regulators. Also utilized in the preparation of specialty polymers and liquid crystals due to its aromatic and functional group compatibility. Its carboxylic acid and chlorine substituent allow for easy derivatization in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿650.00
inventory 5g
10-20 days ฿2,390.00
inventory 25g
10-20 days ฿10,330.00

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3-Chloro-5-methoxybenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It serves as a building block in agrochemicals for developing herbicides and plant growth regulators. Also utilized in the preparation of specialty polymers and liquid crystals due to its aromatic and functional group compatibility. Its carboxylic acid and chlorine substituent allow for easy derivatization in multi-step org

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. It serves as a building block in agrochemicals for developing herbicides and plant growth regulators. Also utilized in the preparation of specialty polymers and liquid crystals due to its aromatic and functional group compatibility. Its carboxylic acid and chlorine substituent allow for easy derivatization in multi-step organic syntheses.

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