Cas no 38550-34-4 (2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane)

2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane is a fluorinated organic compound featuring a perfluorinated carbon chain with an iodine substituent. Its unique structure imparts high chemical and thermal stability, along with hydrophobic and oleophobic properties. The presence of iodine enhances reactivity in substitution and coupling reactions, making it valuable in synthetic chemistry, particularly for introducing perfluorinated segments into target molecules. This compound is also useful in applications requiring inert, non-polar media, such as specialty lubricants or coatings. Its compatibility with fluorinated systems and resistance to degradation under harsh conditions make it a preferred choice in advanced material science and industrial chemistry.
2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane structure
38550-34-4 structure
Product Name:2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane
CAS No:38550-34-4
MF:C9H6F13I
MW:488.02766084671
MDL:MFCD00156018
CID:316560
PubChem ID:2778812
Update Time:2025-05-19

2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane Chemical and Physical Properties

Names and Identifiers

    • Nonane,1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluoro-8-iodo-
    • 1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodononane
    • 1H,1H,1H,2H,3H,3H-Perfluoro-2-iodononane
    • 2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane
    • 1,1,1,2,2,3,3,4,4,5,5,6,6-tridecakis(fluoranyl)-8-iodanyl-nonane
    • 1-(Perfluorohexyl)-2-iodopropane
    • AKOS016015394
    • SCHEMBL9854426
    • EINECS 253-994-5
    • FT-0612651
    • A824186
    • REPFTMOJFHVIBT-UHFFFAOYSA-N
    • MFCD00156018
    • NS00019049
    • DTXSID70880412
    • 38550-34-4
    • MDL: MFCD00156018
    • Inchi: 1S/C9H6F13I/c1-3(23)2-4(10,11)5(12,13)6(14,15)7(16,17)8(18,19)9(20,21)22/h3H,2H2,1H3
    • InChI Key: REPFTMOJFHVIBT-UHFFFAOYSA-N
    • SMILES: IC(C)CC(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F

Computed Properties

  • Exact Mass: 487.93100
  • Monoisotopic Mass: 487.93066g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 0
  • Heavy Atom Count: 23
  • Rotatable Bond Count: 7
  • Complexity: 424
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 6.6
  • Topological Polar Surface Area: 0?2

Experimental Properties

  • Boiling Point: 69 °C
  • PSA: 0.00000
  • LogP: 5.93880

2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane Security Information

  • Hazard Statement: Irritant
  • Hazard Category Code: 36/37/38
  • Safety Instruction: S26; S36
  • Hazardous Material Identification: Xi
  • HazardClass:IRRITANT
  • Risk Phrases:R36/37/38

2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
I736018-50mg
2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane
38550-34-4
50mg
$ 50.00 2022-06-04
TRC
I736018-100mg
2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane
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100mg
$ 65.00 2022-06-04
TRC
I736018-500mg
2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane
38550-34-4
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$ 115.00 2022-06-04
Fluorochem
010323-1g
2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane
38550-34-4 97%
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£32.00 2022-03-01
Apollo Scientific
PC8627-1g
2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane
38550-34-4 97%
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£72.00 2023-09-02
Apollo Scientific
PC8627-5g
2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane
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£157.00 2025-02-22
eNovation Chemicals LLC
Y1265009-1g
2-IODO-1H,1H,1H,2H,3H,3H-PERFLUORONONANE
38550-34-4 97%
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$175 2023-09-01
eNovation Chemicals LLC
Y1265009-5g
2-IODO-1H,1H,1H,2H,3H,3H-PERFLUORONONANE
38550-34-4 97%
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abcr
AB128739-1 g
1H,1H,1H,2H,3H,3H-Perfluoro-2-iodononane, 97%; .
38550-34-4 97%
1 g
€43.50 2023-07-20
abcr
AB128739-5 g
1H,1H,1H,2H,3H,3H-Perfluoro-2-iodononane, 97%; .
38550-34-4 97%
5 g
€109.60 2023-07-20

2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane Related Literature

Additional information on 2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane

Professional Introduction to Compound with CAS No. 38550-34-4 and Product Name: 2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane

2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane, identified by its Chemical Abstracts Service (CAS) number 38550-34-4, is a specialized fluorinated hydrocarbon that has garnered significant attention in the field of organic synthesis and material science. This compound belongs to a class of perfluorinated derivatives, which are characterized by the complete substitution of hydrogen atoms in a carbon chain with fluorine atoms. The presence of an iodine substituent at the second carbon position enhances its utility as a versatile intermediate in synthetic chemistry.

The unique structural features of 2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane make it a valuable building block for the preparation of more complex molecules. The perfluoroalkyl group imparts high thermal stability and chemical inertness, while the iodine atom serves as a reactive handle for further functionalization via cross-coupling reactions. These properties have positioned this compound as a key reagent in the development of advanced materials and pharmaceuticals.

In recent years, the demand for fluorinated compounds has surged due to their exceptional performance in various applications. Perfluorononane derivatives are particularly sought after for their low surface tension and high chemical resistance, making them ideal for use in liquid crystals, lubricants, and high-performance coatings. The introduction of an iodine atom into this framework opens up new possibilities for the synthesis of novel fluorinated polymers and liquid crystalline materials.

One of the most compelling applications of 2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane is in the realm of pharmaceutical research. Fluorinated molecules are widely recognized for their improved metabolic stability and bioavailability. Researchers have leveraged the reactivity of this compound to develop new drug candidates with enhanced pharmacological properties. For instance, recent studies have demonstrated its utility in constructing fluorinated analogs of antiviral and anticancer agents. The ability to introduce fluorine atoms at specific positions while maintaining structural integrity is crucial for optimizing drug efficacy.

The synthesis of 2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane involves sophisticated organic transformations that highlight the intersection of fluorine chemistry and modern synthetic methodologies. Advanced techniques such as palladium-catalyzed cross-coupling reactions and metal-halogen exchange processes are employed to achieve high yields and purity. These synthetic strategies not only underscore the compound's versatility but also reflect the broader trends in synthetic organic chemistry towards more efficient and sustainable practices.

From an industrial perspective, the production of perfluorononane derivatives like 2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane is driven by their potential in emerging technologies. For example, perfluorinated compounds are being explored for their role in energy storage systems due to their ability to function as supercapacitors or electrolytes. The high energy density and stability offered by these materials make them promising candidates for next-generation battery technologies.

The environmental impact of fluorinated chemicals is also a critical consideration in their development and application. While perfluorinated compounds are known for their durability and resistance to degradation, concerns about their persistence in ecosystems have led to research focused on greener alternatives. Innovations in synthetic chemistry aim to minimize waste and reduce hazardous byproducts during the production process. This aligns with global efforts to promote sustainable manufacturing practices across all industries.

Future research directions for 2-Iodo-1H,1H,1H,2H,3H,3H-perfluorononane may include exploring its role in polymer science and nanotechnology. The compound's unique properties could enable the development of novel materials with tailored functionalities for applications ranging from electronics to biomedical devices. Collaborative efforts between chemists and engineers will be essential to translate laboratory discoveries into practical solutions.

In conclusion,2-Iodo-1H,1H,H????????perflurononane (CAS No. 38550-34-4) represents a significant advancement in fluorinated chemistry with broad implications across multiple disciplines. Its synthesis reflects cutting-edge methodologies while its applications span pharmaceuticals to advanced materials. As research continues to uncover new uses for this compound,perflurononanederivatives will undoubtedly play an increasingly important role in shaping innovation in science and technology.

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