2-Amino-3-chloro-5-trifluoromethyl-benzoic acid methyl ester

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Reagent Code: #133438
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CAS Number 1806927-85-4

science Other reagents with same CAS 1806927-85-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.6056 g/mol
Formula C₉H₇ClF₃NO₂
badge Registry Numbers
MDL Number MFCD28721371
thermostat Physical Properties
Boiling Point 277.6±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.448±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs. It serves as a building block in the production of certain antipsychotic and antidepressant medications due to its ability to form complex heterocyclic structures. Its chloro and trifluoromethyl groups enhance reactivity and binding selectivity in drug molecules. Also employed in agrochemical synthesis for creating herbicides and plant growth regulators, where its aromatic and functional group arrangement contributes to biological activity. Commonly utilized in research laboratories for structure-activity relationship (SAR) studies in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,000.00
inventory 250mg
10-20 days ฿22,400.00
inventory 1g
10-20 days ฿44,800.00

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2-Amino-3-chloro-5-trifluoromethyl-benzoic acid methyl ester
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs. It serves as a building block in the production of certain antipsychotic and antidepressant medications due to its ability to form complex heterocyclic structures. Its chloro and trifluoromethyl groups enhance reactivity and binding selectivity in drug molecules. Also employed in agrochemical synthesis for creating herbicides and plant growth regulators, where its aromatic and functional group arrangement contributes to biological activity. Commonly utilized in research laboratories for structure-activity relationship (SAR) studies in medicinal chemistry.
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