Cas no 1804519-05-8 (2,4-Diiodo-3-fluorotoluene)

2,4-Diiodo-3-fluorotoluene structure
2,4-Diiodo-3-fluorotoluene structure
Product Name:2,4-Diiodo-3-fluorotoluene
CAS No:1804519-05-8
MF:C7H5FI2
MW:361.921950101852
CID:5006563
Update Time:2025-07-20

2,4-Diiodo-3-fluorotoluene Chemical and Physical Properties

Names and Identifiers

    • 2,4-Diiodo-3-fluorotoluene
    • Inchi: 1S/C7H5FI2/c1-4-2-3-5(9)6(8)7(4)10/h2-3H,1H3
    • InChI Key: RZDSPAJWSXPICF-UHFFFAOYSA-N
    • SMILES: IC1C(=C(C=CC=1C)I)F

Computed Properties

  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 0
  • Complexity: 118
  • XLogP3: 3.7
  • Topological Polar Surface Area: 0

2,4-Diiodo-3-fluorotoluene Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Alichem
A010007397-250mg
2,4-Diiodo-3-fluorotoluene
1804519-05-8 97%
250mg
480.00 USD 2021-07-06
Alichem
A010007397-500mg
2,4-Diiodo-3-fluorotoluene
1804519-05-8 97%
500mg
782.40 USD 2021-07-06
Alichem
A010007397-1g
2,4-Diiodo-3-fluorotoluene
1804519-05-8 97%
1g
1,534.70 USD 2021-07-06

Additional information on 2,4-Diiodo-3-fluorotoluene

Comprehensive Analysis of 2,4-Diiodo-3-fluorotoluene (CAS No. 1804519-05-8): Properties, Applications, and Industry Trends

2,4-Diiodo-3-fluorotoluene (CAS No. 1804519-05-8) is a halogenated aromatic compound that has garnered significant attention in the fields of organic synthesis, pharmaceuticals, and material science. This compound, characterized by its unique diiodo-fluorotoluene structure, serves as a versatile intermediate in the development of advanced chemical entities. With the increasing demand for fluorinated compounds and iodinated building blocks, this chemical has become a focal point for researchers and industry professionals alike.

The molecular structure of 2,4-Diiodo-3-fluorotoluene features two iodine atoms at the 2- and 4-positions and a fluorine atom at the 3-position of the toluene ring. This arrangement imparts distinct electronic and steric properties, making it highly valuable for cross-coupling reactions, such as Suzuki-Miyaura and Sonogashira couplings. These reactions are pivotal in the synthesis of complex molecules, including pharmaceutical intermediates and agrochemicals. Recent studies highlight its role in the development of bioactive molecules, particularly in the context of drug discovery and medicinal chemistry.

In the context of current industry trends, the demand for halogenated aromatic compounds like 2,4-Diiodo-3-fluorotoluene is driven by their utility in high-performance materials. For instance, they are employed in the synthesis of liquid crystals, organic semiconductors, and polymeric materials used in electronics and optoelectronics. The compound's ability to act as a precursor in these applications underscores its importance in advancing green chemistry and sustainable manufacturing practices.

From a regulatory and safety perspective, 2,4-Diiodo-3-fluorotoluene is handled under standard laboratory protocols to ensure safe usage. Its stability and compatibility with various solvents make it a reliable choice for industrial-scale synthesis. Researchers often inquire about its storage conditions, handling precautions, and compatibility with other reagents, which are critical for optimizing reaction yields and minimizing waste.

The growing interest in fluorinated and iodinated compounds has also led to increased searches for synthetic routes and alternative methodologies to produce 2,4-Diiodo-3-fluorotoluene efficiently. Innovations in catalytic processes and flow chemistry have further enhanced its accessibility, reducing production costs and environmental impact. These advancements align with the broader shift toward eco-friendly chemical synthesis and circular economy principles.

In summary, 2,4-Diiodo-3-fluorotoluene (CAS No. 1804519-05-8) stands as a critical component in modern chemical research and industrial applications. Its multifaceted utility in pharmaceuticals, materials science, and organic synthesis positions it as a compound of enduring relevance. As the scientific community continues to explore its potential, this compound is poised to play a pivotal role in addressing contemporary challenges in chemical innovation and sustainable development.

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