Methyl 5-chloro-2-iodobenzoate

≥95%

Reagent Code: #120010
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CAS Number 289039-82-3

science Other reagents with same CAS 289039-82-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.49 g/mol
Formula C₈H₆ClIO₂
badge Registry Numbers
MDL Number MFCD00144772
thermostat Physical Properties
Boiling Point 295.649°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed away from light

description Product Description

This compound is primarily utilized in organic synthesis as a versatile building block for constructing more complex molecules. Its structure, featuring both chloro and iodo substituents, makes it a valuable intermediate in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are widely employed in pharmaceutical and agrochemical research. Additionally, the ester group in the molecule allows for further functionalization, enabling the synthesis of various derivatives for use in drug discovery and material science. Its reactivity and stability make it a suitable candidate for developing compounds with potential biological activity or specialized industrial applications.

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Test Parameter Specification
Appearance Yellow Liquid
Purity (%) 95-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿270.00
inventory 5g
10-20 days ฿2,493.00
inventory 1g
10-20 days ฿765.00

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Methyl 5-chloro-2-iodobenzoate
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This compound is primarily utilized in organic synthesis as a versatile building block for constructing more complex molecules. Its structure, featuring both chloro and iodo substituents, makes it a valuable intermediate in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are widely employed in pharmaceutical and agrochemical research. Additionally, the ester group in the molecule allows for further functionalization, enabling the synthesis of various derivatives for use in drug d

This compound is primarily utilized in organic synthesis as a versatile building block for constructing more complex molecules. Its structure, featuring both chloro and iodo substituents, makes it a valuable intermediate in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are widely employed in pharmaceutical and agrochemical research. Additionally, the ester group in the molecule allows for further functionalization, enabling the synthesis of various derivatives for use in drug discovery and material science. Its reactivity and stability make it a suitable candidate for developing compounds with potential biological activity or specialized industrial applications.

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