methyl 2-(chlorocarbonyl)benzoate

≥96.5% (HPLC); 96.5-103.5% (AT); 97%

Reagent Code: #209779
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CAS Number 4397-55-1

science Other reagents with same CAS 4397-55-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.60 g/mol
Formula C₉H₇ClO₃
badge Registry Numbers
MDL Number MFCD11656039
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inflatable

description Product Description

Methyl 2-(chlorocarbonyl)benzoate is a specialty chemical intermediate used in organic synthesis, particularly for pharmaceuticals, agrochemicals, and fine chemicals. As a bifunctional reagent featuring an acid chloride and an ortho-methyl ester group, it facilitates the introduction of the 2-(methoxycarbonyl)benzoyl moiety into molecules. It reacts with nucleophiles such as amines to form amides, enabling the construction of heterocyclic compounds and complex ring systems. Commonly applied in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), dyes, and other bioactive molecules, its ortho substitution allows for directed cyclization reactions and selective functional group transformations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿12,840.00
inventory 5g
10-20 days ฿44,470.00
methyl 2-(chlorocarbonyl)benzoate
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Methyl 2-(chlorocarbonyl)benzoate is a specialty chemical intermediate used in organic synthesis, particularly for pharmaceuticals, agrochemicals, and fine chemicals. As a bifunctional reagent featuring an acid chloride and an ortho-methyl ester group, it facilitates the introduction of the 2-(methoxycarbonyl)benzoyl moiety into molecules. It reacts with nucleophiles such as amines to form amides, enabling the construction of heterocyclic compounds and complex ring systems. Commonly applied in the synthesis
Methyl 2-(chlorocarbonyl)benzoate is a specialty chemical intermediate used in organic synthesis, particularly for pharmaceuticals, agrochemicals, and fine chemicals. As a bifunctional reagent featuring an acid chloride and an ortho-methyl ester group, it facilitates the introduction of the 2-(methoxycarbonyl)benzoyl moiety into molecules. It reacts with nucleophiles such as amines to form amides, enabling the construction of heterocyclic compounds and complex ring systems. Commonly applied in the synthesis of non-steroidal anti-inflammatory drugs (NSAIDs), dyes, and other bioactive molecules, its ortho substitution allows for directed cyclization reactions and selective functional group transformations.
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