Methyl 3-chloro-5-fluorobenzoate

95%

Reagent Code: #66277
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CAS Number 327056-75-7

science Other reagents with same CAS 327056-75-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.58 g/mol
Formula C₈H₆ClFO₂
badge Registry Numbers
MDL Number MFCD06204128
thermostat Physical Properties
Boiling Point 237.143°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a building block for more complex molecules. Its structure, featuring both chloro and fluoro substituents, makes it a valuable intermediate in the development of pharmaceuticals and agrochemicals. The ester group allows for further chemical modifications, enabling the creation of various derivatives with potential biological activity. Additionally, it serves as a precursor in the synthesis of specialty chemicals used in research and industrial applications, particularly in the fields of medicinal chemistry and material science. Its unique substitution pattern also makes it useful in studies involving structure-activity relationships (SAR) to optimize the efficacy of active compounds.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,613.00
inventory 1g
10-20 days ฿4,302.00

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Methyl 3-chloro-5-fluorobenzoate
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This compound is primarily utilized in organic synthesis as a building block for more complex molecules. Its structure, featuring both chloro and fluoro substituents, makes it a valuable intermediate in the development of pharmaceuticals and agrochemicals. The ester group allows for further chemical modifications, enabling the creation of various derivatives with potential biological activity. Additionally, it serves as a precursor in the synthesis of specialty chemicals used in research and industrial applications, particularly in the fields of medicinal chemistry and material science. Its unique substitution pattern also makes it useful in studies involving structure-activity relationships (SAR) to optimize the efficacy of active compounds.
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