2-Iodo-6-(trifluoromethyl)pyridin-3-amine

≥95%

Reagent Code: #200233
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CAS Number 920979-04-0

science Other reagents with same CAS 920979-04-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.01 g/mol
Formula C₆H₄F₃IN₂
badge Registry Numbers
MDL Number MFCD11044265
thermostat Physical Properties
Boiling Point 233.1°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in medicinal chemistry. Also employed in agrochemicals to create novel pesticides with improved efficacy and environmental profiles. Commonly utilized in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to form carbon-nitrogen or carbon-carbon bonds in complex molecule assembly.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿880.00
inventory 1g
10-20 days ฿3,130.00
inventory 5g
10-20 days ฿15,620.00

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2-Iodo-6-(trifluoromethyl)pyridin-3-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in medicinal chemistry. Also employed in agrochemicals to create novel pesticides with improved efficacy and environmental profiles. Commonly utilized in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to form carbon-nitrogen or carbon-carbon bonds in complex molecule as

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective binding in biological systems, making it valuable in medicinal chemistry. Also employed in agrochemicals to create novel pesticides with improved efficacy and environmental profiles. Commonly utilized in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig, to form carbon-nitrogen or carbon-carbon bonds in complex molecule assembly.

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