Ethyl 4-chlorobenzoate

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Reagent Code: #182019
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CAS Number 7335-27-5

science Other reagents with same CAS 7335-27-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.62 g/mol
Formula C₉H₉ClO₂
badge Registry Numbers
MDL Number MFCD00013645
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of active ingredients in certain drugs due to its ester functionality and halogen substituent, which allow further chemical modifications. Commonly employed in organic reactions such as nucleophilic substitutions and coupling reactions. Also utilized in the development of dyes and specialty polymers where aromatic ester groups enhance stability and reactivity. Its role as a building block makes it valuable in research laboratories for constructing more complex molecules.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿310.00
inventory 100g
10-20 days ฿511.50
inventory 500g
10-20 days ฿4,630.00
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Ethyl 4-chlorobenzoate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of active ingredients in certain drugs due to its ester functionality and halogen substituent, which allow further chemical modifications. Commonly employed in organic reactions such as nucleophilic substitutions and coupling reactions. Also utilized in the development of dyes and specialty polymers where aromatic ester groups enhance stability and reactivity. Its role as a building block makes it

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves in the preparation of active ingredients in certain drugs due to its ester functionality and halogen substituent, which allow further chemical modifications. Commonly employed in organic reactions such as nucleophilic substitutions and coupling reactions. Also utilized in the development of dyes and specialty polymers where aromatic ester groups enhance stability and reactivity. Its role as a building block makes it valuable in research laboratories for constructing more complex molecules.

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