Ethyl 4-ethyl-3-iodobenzoate

≥98%

Reagent Code: #83848
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CAS Number 1131588-09-4

science Other reagents with same CAS 1131588-09-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 304.12 g/mol
Formula C₁₁H₁₃IO₂
badge Registry Numbers
MDL Number MFCD11112910
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Ethyl 4-ethyl-3-iodobenzoate is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both an ethyl ester group and an iodine substituent, makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings. These reactions are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the compound can serve as a building block for the synthesis of complex organic molecules, particularly in medicinal chemistry, where it may contribute to the creation of drug candidates or biologically active compounds. Its iodine atom also allows for easy modification or labeling in research applications.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance yellow liquid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿3,690.00
1g
10-20 days ฿9,070.00
5g
10-20 days ฿28,800.00
Ethyl 4-ethyl-3-iodobenzoate
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Ethyl 4-ethyl-3-iodobenzoate is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both an ethyl ester group and an iodine substituent, makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings. These reactions are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the compound can serve as a building block for the synthesis of complex organic molec

Ethyl 4-ethyl-3-iodobenzoate is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring both an ethyl ester group and an iodine substituent, makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings. These reactions are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the compound can serve as a building block for the synthesis of complex organic molecules, particularly in medicinal chemistry, where it may contribute to the creation of drug candidates or biologically active compounds. Its iodine atom also allows for easy modification or labeling in research applications.

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