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重要文件

473863

Sigma-Aldrich

八氟-1,4-二碘丁烷

98%

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About This Item

線性公式:
I(CF2)4I
CAS號碼:
分子量::
453.84
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

98%

折射率

n20/D 1.429 (lit.)

bp

150 °C (lit.)

mp

−9 °C (lit.)

密度

2.474 g/mL at 25 °C (lit.)

官能基

fluoro
iodo

SMILES 字串

FC(F)(I)C(F)(F)C(F)(F)C(F)(F)I

InChI

1S/C4F8I2/c5-1(6,3(9,10)13)2(7,8)4(11,12)14

InChI 密鑰

JILAKKYYZPDQBE-UHFFFAOYSA-N

一般說明

Octafluoro-1,4-diiodobutane (ofib, C4F8I2) is also referred to as 1,1,2,2,3,3,4,4-octafluoro-1,4-diiodobutane. It acts as a halogen bond donor compound and its cocrystallization with methyldiphenylphosphine oxide (mdppo) has been investigated. In combination with a calixcrown compound ofib forms a ′binary host′ system, which is employed for the isolation of cesium iodide from aqueous to fluorous phase.

應用

Octafluoro-1,4-diiodobutane may be used as a guest molecule to prepare a chiral bidentate inclusion complex with pyridyl moieties of a pyridoallenoacetylenic host. It may be employed in the synthesis of three-component supramolecular complexes.

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Silvia Castro-Fernández et al.
Organic letters, 16(4), 1136-1139 (2014-02-12)
A chiral bidentate inclusion complex has been formed by halogen-bond interaction between the pyridyl moieties of a pyridoallenoacetylenic host and octafluorodiiodobutane. X-ray crystallography showed that the guest adopts a chiral conformation inside the molecular channels formed by stacking of the
Switching between halogen-and hydrogen-bonding in stoichiometric variations of a cocrystal of a phosphine oxide.
Oh SY, et al.
CrystEngComm, 14(19), 6110-6114 (2012)
Dipyridinocalixcrown/diiodoperfluorocarbon binary host systems for CsI: structural studies and fluorous phase extraction of caesium.
Gattuso G, et al.
Tetrahedron, 63(23), 4951-4958 (2007)
Metric engineering of supramolecular Borromean rings.
Liantonio R, et al.
Chemical Communications (Cambridge, England), 17, 1819-1821 (2006)
Liang Lu et al.
Journal of applied toxicology : JAT, 39(7), 945-954 (2019-03-06)
Fluorinated diiodine alkanes (FDIAs), important industrial intermediates in the synthesis of various perfluorinated compounds, which are distributed widely in wildlife and humans. Recent studies showed that FDIAs had in vitro estrogenic effects. However, to date, little information is available regarding

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