Ethyl 4-chloro-2-iodobenzoate

95%

Reagent Code: #184710
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CAS Number 1020174-06-4

science Other reagents with same CAS 1020174-06-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 310.52 g/mol
Formula C₉H₈ClIO₂
badge Registry Numbers
MDL Number MFCD12024994
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for selective functionalization on the aromatic ring, making it valuable in medicinal chemistry for constructing complex organic molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or alkenyl groups. Also utilized in the preparation of agrochemicals and specialty materials where halogenated aromatic esters serve as key building blocks.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿560.00
inventory 5g
10-20 days ฿5,950.00
inventory 25g
10-20 days ฿25,740.00
inventory 1g
10-20 days ฿1,390.00
Ethyl 4-chloro-2-iodobenzoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for selective functionalization on the aromatic ring, making it valuable in medicinal chemistry for constructing complex organic molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or alkenyl groups. Also utilized in the preparation of agrochemicals and specia
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its structure allows for selective functionalization on the aromatic ring, making it valuable in medicinal chemistry for constructing complex organic molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or alkenyl groups. Also utilized in the preparation of agrochemicals and specialty materials where halogenated aromatic esters serve as key building blocks.
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