Methyl 4-chloro-2-methylbenzoate

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Reagent Code: #47113
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CAS Number 99585-12-3

science Other reagents with same CAS 99585-12-3

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Weight 184.6196 g/mol
Formula C₉H₉ClO₂
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MDL Number MFCD09842344
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Methyl 4-chloro-2-methylbenzoate is primarily used as an intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Its structure makes it a valuable building block for creating more complex molecules, such as active ingredients in medications or pesticides. In the pharmaceutical industry, it can be utilized in the development of drugs targeting specific biological pathways, owing to its benzoate ester functionality. Additionally, it serves as a key reagent in chemical research for studying reaction mechanisms or developing new synthetic methodologies. Its applications also extend to the production of dyes, fragrances, and other specialty chemicals, where its aromatic and ester properties are leveraged for specific functional roles.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,449.00

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Methyl 4-chloro-2-methylbenzoate
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Methyl 4-chloro-2-methylbenzoate is primarily used as an intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Its structure makes it a valuable building block for creating more complex molecules, such as active ingredients in medications or pesticides. In the pharmaceutical industry, it can be utilized in the development of drugs targeting specific biological pathways, owing to its benzoate ester functionality. Additionally, it s

Methyl 4-chloro-2-methylbenzoate is primarily used as an intermediate in the synthesis of various organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Its structure makes it a valuable building block for creating more complex molecules, such as active ingredients in medications or pesticides. In the pharmaceutical industry, it can be utilized in the development of drugs targeting specific biological pathways, owing to its benzoate ester functionality. Additionally, it serves as a key reagent in chemical research for studying reaction mechanisms or developing new synthetic methodologies. Its applications also extend to the production of dyes, fragrances, and other specialty chemicals, where its aromatic and ester properties are leveraged for specific functional roles.

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