5-iodo-3-nitropyridin-2-amine

≥95%

Reagent Code: #199505
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CAS Number 25391-57-5

science Other reagents with same CAS 25391-57-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.01 g/mol
Formula C₅H₄IN₃O₂
badge Registry Numbers
MDL Number MFCD04038464
thermostat Physical Properties
Melting Point 215-219 °C
Boiling Point 365.4 °C at 760 mmHg
inventory_2 Storage & Handling
Density 2.229±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions due to the presence of the iodine moiety, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the preparation of agrochemicals and bioactive molecules where nitro and amino groups serve as handles for further transformation.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿510.00
inventory 5g
10-20 days ฿1,350.00
inventory 25g
10-20 days ฿5,390.00
inventory 100g
10-20 days ฿20,480.00
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5-iodo-3-nitropyridin-2-amine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions due to the presence of the iodine moiety, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the preparation of agrochemicals and bioactive mole

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating targeted drug candidates. Commonly employed in cross-coupling reactions due to the presence of the iodine moiety, enabling the formation of carbon-carbon and carbon-heteroatom bonds. Also utilized in the preparation of agrochemicals and bioactive molecules where nitro and amino groups serve as handles for further transformation.

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