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Catalog Number:
46031
CAS Number:
141743-49-9
2,6-Difluoro-4-yodoanilina
Purity:
≥ 98% (GC)
Synonym(s):
2,6-Difluoro-4-yodobencenamina
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Product Information

2,6-Difluoro-4-iodoaniline is a versatile chemical compound with significant applications in the fields of pharmaceuticals and agrochemicals. This compound is recognized for its unique fluorine and iodine substituents, which enhance its reactivity and make it a valuable intermediate in the synthesis of various biologically active molecules. Researchers utilize 2,6-Difluoro-4-iodoaniline in the development of novel drug candidates, particularly in the creation of targeted therapies for cancer and other diseases. Its ability to modify biological pathways makes it a crucial component in medicinal chemistry.

Moreover, 2,6-Difluoro-4-iodoaniline is also employed in the formulation of advanced agrochemicals, contributing to the development of effective pesticides and herbicides. Its distinctive properties allow for improved efficacy and selectivity in agricultural applications, ensuring better crop protection while minimizing environmental impact. With its dual functionality in both pharmaceutical and agricultural sectors, 2,6-Difluoro-4-iodoaniline stands out as a compound of choice for researchers and industry professionals seeking innovative solutions.

Synonyms
2,6-Difluoro-4-yodobencenamina
CAS Number
141743-49-9
Purity
≥ 98% (GC)
Molecular Formula
C 6 H 4 F 2 PULGADAS
Molecular Weight
255.01
MDL Number
MFCD07774189
PubChem ID
278943
Melting Point
80 - 84 °C
Appearance
Polvo de color blanco a amarillo claro a naranja claro hasta cristal.
Conditions
Tienda en RT
General Information
Synonyms
2,6-Difluoro-4-yodobencenamina
CAS Number
141743-49-9
Purity
≥ 98% (GC)
Molecular Formula
C 6 H 4 F 2 PULGADAS
Molecular Weight
255.01
MDL Number
MFCD07774189
PubChem ID
278943
Melting Point
80 - 84 °C
Appearance
Polvo de color blanco a amarillo claro a naranja claro hasta cristal.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,6-Difluoro-4-iodoaniline is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting specific diseases. Its unique halogen substitutions enhance biological activity and selectivity.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, including herbicides and fungicides, providing effective solutions for crop protection while minimizing environmental impact.
  • Material Science: The compound is explored in the development of advanced materials, such as polymers and coatings, due to its ability to modify physical properties and improve durability.
  • Organic Synthesis: Researchers utilize this chemical in organic synthesis for creating complex molecules, benefiting from its reactivity and functional group compatibility, which can streamline multi-step reactions.
  • Analytical Chemistry: It is employed as a standard in analytical methods, aiding in the detection and quantification of similar compounds in various samples, thus enhancing accuracy in research and quality control.

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