2253-14-7

Basic information

• Product Name: 1-IODO-1H,1H-NONAFLUOROPENTANE
• Synonyms: 1-IODO-1H,1H-NONAFLUOROPENTANE;1-Iodo-2,2,3,3,4,4,5,5,5-nonafluoropentane;1-IODO-1H,1H-NONAFLUOROPENTANE, 97% MIN.;1-Iodo-1H,1H-perfluoropentane;1H,1H-Perfluoropentyl iodide, 1-Iodo-1H,1H-nonafluoropentane
• CAS NO: 2253-14-7
• Molecular Formula: C₅H₂F₉I
• Molecular Weight: 359.96
• Mol File: 2253-14-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 118.7 °C at 760 mmHg
• Flash Point: 42.8 °C
• Appearance: /
• Density: 2.009 g/cm³
• Vapor Pressure: 19.7mmHg at 25°C
• Refractive Index: 1.359
• CAS DataBase Reference: 1-IODO-1H,1H-NONAFLUOROPENTANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-IODO-1H,1H-NONAFLUOROPENTANE(2253-14-7)
• EPA Substance Registry System: 1-IODO-1H,1H-NONAFLUOROPENTANE(2253-14-7)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 2253-14-7(Hazardous Substances Data)

Usage

General Description

1-Iodo-1H,1H-nonafluoropentane is a specialty chemical with the molecular formula C5HF9I. 1-IODO-1H,1H-NONAFLUOROPENTANE belongs to the class of organic compounds known as halohydrocarbons. Specifically, it is a fluorocarbon halide and iodohydrocarbon that is often used in industrial applications. It typically appears as a clear, colorless liquid under normal conditions. In terms of its physical and chemical properties, it is non-flammable, stable, and not reactive with water, making it suitable for certain specialized uses in scientific research and industries including electronics, pharmaceuticals, and plastics. However, it may pose hazards if not handled properly, as it can be harmful if inhaled, causes skin and eye irritation, and may cause damage to organs through prolonged or repeated exposure.

InChI:InChI=1/C5H2F9I/c6-2(7,1-15)3(8,9)4(10,11)5(12,13)14/h1H2

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Relevant articles and documents

Bi- and tridentate silicon-based acceptor molecules

Triethynylphenylsilane (1), trivinylphenylsilane (2), diethynyldiphenylsilane (3) and diphenyldivinylsilane (4) were reacted with chlorodimethylsilane yielding the corresponding hydrosilylation products. To increase their Lewis acidity, the Si-Cl functions were directly transferred into Si-C6F5 units by salt elimination reactions leading to the (semi-) flexible molecules 5-8 bearing two or three Lewis-acidic sidearms. With the aim of providing host-guest complexes, the air-stable and readily soluble compounds 5-8 were converted with N- and O-Lewis bases of different size and geometry. In all cases, NMR spectroscopic investigations reveal no formation of Lewis acid-base complexes. X-ray diffraction experiments of host compounds 5-7 show intermolecular aryl perfluoroaryl interactions of dispersion nature in the solid state. By hydrosilylation of 1 with trichlorosilane the more Lewisacidic all-trans-tris[(trichlorosilyl)vinyl]phenylsilane (9) was obtained. Its Lewis acidity was further increased by fluorination to yield all-trans-tris[(trifluorosilyl)vinyl] phenylsilane (10); the conversion with nitrogen containing Lewis bases ends up in the formation of insoluble precipitates.

NOVEL COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME

Compounds represented by Formula 1 and organic light-emitting devices including an organic layer including the compounds are disclosed.