4-Iodo-2-nitroaniline

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Reagent Code: #199611
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CAS Number 20691-72-9

science Other reagents with same CAS 20691-72-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.02 g/mol
Formula C₆H₅IN₂O₂
badge Registry Numbers
MDL Number MFCD06808526
thermostat Physical Properties
Melting Point 120-123 °C(lit.)
Boiling Point 352.9±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.101±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of advanced heterocyclic compounds. Its structure allows for selective functionalization in multi-step organic reactions. Commonly employed in the development of dyes and pigments due to its nitro and amino groups, which contribute to chromophoric properties. Also utilized in research settings for the preparation of labeled compounds in medicinal chemistry, where the iodine atom enables further transformations via cross-coupling reactions such as Suzuki or Heck reactions.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿1,320.00
inventory 25g
10-20 days ฿3,010.00

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4-Iodo-2-nitroaniline
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of advanced heterocyclic compounds. Its structure allows for selective functionalization in multi-step organic reactions. Commonly employed in the development of dyes and pigments due to its nitro and amino groups, which contribute to chromophoric properties. Also utilized in research settings for the preparation of labeled compounds in medicinal chemistry, where the iodine atom enables further

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the preparation of advanced heterocyclic compounds. Its structure allows for selective functionalization in multi-step organic reactions. Commonly employed in the development of dyes and pigments due to its nitro and amino groups, which contribute to chromophoric properties. Also utilized in research settings for the preparation of labeled compounds in medicinal chemistry, where the iodine atom enables further transformations via cross-coupling reactions such as Suzuki or Heck reactions.

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