Ethyl 3-nitrobenzoate

95%

Reagent Code: #185320
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CAS Number 618-98-4

science Other reagents with same CAS 618-98-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.18 g/mol
Formula C₉H₉NO₄
badge Registry Numbers
MDL Number MFCD00014702
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for introducing the nitrobenzoate moiety into more complex molecules. Commonly employed in the development of active pharmaceutical ingredients where the nitro group can be reduced to an amine for further functionalization. Also utilized in the synthesis of dyes and specialty esters due to its reactivity in nucleophilic substitution and esterification reactions. Its electron-withdrawing nitro group enhances the compound’s utility in Michael addition and other carbon-carbon bond-forming reactions.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿960.00
inventory 100g
10-20 days ฿2,980.00
inventory 500g
10-20 days ฿12,980.00
Ethyl 3-nitrobenzoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for introducing the nitrobenzoate moiety into more complex molecules. Commonly employed in the development of active pharmaceutical ingredients where the nitro group can be reduced to an amine for further functionalization. Also utilized in the synthesis of dyes and specialty esters due to its reactivity in nucleophilic substitution and esterification reactions

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for introducing the nitrobenzoate moiety into more complex molecules. Commonly employed in the development of active pharmaceutical ingredients where the nitro group can be reduced to an amine for further functionalization. Also utilized in the synthesis of dyes and specialty esters due to its reactivity in nucleophilic substitution and esterification reactions. Its electron-withdrawing nitro group enhances the compound’s utility in Michael addition and other carbon-carbon bond-forming reactions.

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