2,3-Difluoro-6-iodoaniline

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Reagent Code: #131134
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CAS Number 1807085-17-1

science Other reagents with same CAS 1807085-17-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255 g/mol
Formula C₆H₄F₂IN
badge Registry Numbers
MDL Number MFCD28789173
thermostat Physical Properties
Boiling Point 238.7±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.086±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated active pharmaceutical ingredients (APIs) where the fluorine atoms enhance metabolic stability and bioavailability. Its iodo functionality allows for further coupling reactions, such as Suzuki or Buchwald-Hartwig, enabling the construction of complex aromatic systems in drug candidates. Commonly employed in research and development for oncology and central nervous system (CNS) drugs due to its ability to fine-tune lipophilicity and binding affinity. Also utilized in agrochemical synthesis for creating novel herbicides and pesticides with improved environmental profiles.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,990.00
inventory 5g
10-20 days ฿17,490.00

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2,3-Difluoro-6-iodoaniline
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated active pharmaceutical ingredients (APIs) where the fluorine atoms enhance metabolic stability and bioavailability. Its iodo functionality allows for further coupling reactions, such as Suzuki or Buchwald-Hartwig, enabling the construction of complex aromatic systems in drug candidates. Commonly employed in research and development for oncology and central nervous system (CNS) drugs due to its ab

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated active pharmaceutical ingredients (APIs) where the fluorine atoms enhance metabolic stability and bioavailability. Its iodo functionality allows for further coupling reactions, such as Suzuki or Buchwald-Hartwig, enabling the construction of complex aromatic systems in drug candidates. Commonly employed in research and development for oncology and central nervous system (CNS) drugs due to its ability to fine-tune lipophilicity and binding affinity. Also utilized in agrochemical synthesis for creating novel herbicides and pesticides with improved environmental profiles.

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