2-Iodo-4-nitrophenol

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Reagent Code: #200417
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CAS Number 89487-91-2

science Other reagents with same CAS 89487-91-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.0053 g/mol
Formula C₆H₄INO₃
badge Registry Numbers
MDL Number MFCD01165664
thermostat Physical Properties
Melting Point 89-94 °C
Boiling Point 294.5 °C at 760 mmHg
inventory_2 Storage & Handling
Density 2.176 g/cm3
Storage 2-8°C

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 iodo and nitro functional groups into more complex molecules. The compound is also employed in the development of dyes and pigments due to its aromatic nitro structure. Its iodo functionality allows for coupling reactions, such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for constructing biaryl systems. Additionally, it has been explored in the synthesis of antimicrobial agents and other bioactive compounds where the nitrophenol moiety contributes to biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,590.00
inventory 1g
10-20 days ฿4,750.00
inventory 5g
10-20 days ฿22,880.00

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2-Iodo-4-nitrophenol
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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 iodo and nitro functional groups into more complex molecules. The compound is also employed in the development of dyes and pigments due to its aromatic nitro structure. Its iodo functionality allows for coupling reactions, such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for constructing biaryl systems. Additionally, i

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for introducing iodo and nitro functional groups into more complex molecules. The compound is also employed in the development of dyes and pigments due to its aromatic nitro structure. Its iodo functionality allows for coupling reactions, such as Suzuki or Heck reactions, making it valuable in medicinal chemistry for constructing biaryl systems. Additionally, it has been explored in the synthesis of antimicrobial agents and other bioactive compounds where the nitrophenol moiety contributes to biological activity.

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