About This Item
Produtos recomendados
pressão de vapor
3.8 mmHg ( 25 °C)
pf
129 °C (lit.)
densidade
4.32 g/mL at 25 °C (lit.)
cadeia de caracteres SMILES
F[Xe]F
InChI
1S/F2Xe/c1-3-2
chave InChI
IGELFKKMDLGCJO-UHFFFAOYSA-N
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Aplicação
Very useful fluorination agent.
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 1 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Ox. Sol. 2 - Skin Corr. 1B
Código de classe de armazenamento
5.1B - Oxidizing hazardous materials
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Fluorination with XeF(2).(1) 44. Effect of Geometry and Heteroatom on the Regioselectivity of Fluorine Introduction into an Aromatic Ring.
The Journal of organic chemistry, 63(3), 878-880 (2001-10-24)
Angewandte Chemie (International ed. in English), 48(8), 1432-1434 (2009-01-14)
Noble molecule: [Mg(XeF(2))(XeF(4))](AsF(6))(2) is the first coordination compound in which XeF(4) acts as a ligand to a metal center. It is also the first known compound, in which XeF(2) and XeF(4) are simultaneously coordinated to the same metal center (see
Biomedical microdevices, 10(2), 179-186 (2007-09-25)
The majority of microfluidic devices employ networks of channels that have rectangular cross-sections. At the microvascular scale of 30 to 300 microm in diameter, however, the distribution of fluid mechanical stresses and the induced shape of cultured cells will be
Journal of vascular surgery, 3(2), 284-287 (1986-02-01)
Laser angioplasty has been limited by the lack of precise control of thermal and acoustic vascular injury. Pulsed excimer lasers, by contrast, have a capacity to affect target tissue without heat dispersion or damage to surrounding structures. The ablative properties
Inorganic chemistry, 47(1), 5-7 (2007-12-07)
Palladium(II) aryliodo complexes bearing chelating diphosphine ligands react with XeF2, giving iodoarene and rare palladium(II) difluoro complexes. The reaction is general with regard to the aryl group, with even C6F5-I undergoing facile reductive elimination from a Pd center.
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