44028
环己烯
analytical standard, ≥99.5% (GC)
别名:
四氢化苯
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关于此项目
经验公式（希尔记法）:
C6H10
化学文摘社编号:
分子量:
82.14
NACRES:
NA.24
PubChem Substance ID:
EC Number:
203-807-8
Beilstein/REAXYS Number:
906737
MDL number:
UNSPSC Code:
12141716
InChI
1S/C6H10/c1-2-4-6-5-3-1/h1-2H,3-6H2
InChI key
HGCIXCUEYOPUTN-UHFFFAOYSA-N
SMILES string
C1CCC=CC1
grade
analytical standard
vapor density
2.8 (vs air)
vapor pressure
160 mmHg ( 20 °C)
assay
≥99.5% (GC)
autoignition temp.
590 °F
shelf life
limited shelf life, expiry date on the label
contains
~0.01% 2,6-di-tert-butyl-4-methylphenol as stabilizer
expl. lim.
5 %
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
Quality Level
bp
83 °C (lit.)
mp
−104 °C (lit.)
density
0.811 g/mL at 25 °C (lit.)
application(s)
environmental
petroleum
format
neat
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
1.4 °F
flash_point_c
-17 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Amelia W Ray et al.
The journal of physical chemistry. A, 116(25), 6720-6730 (2012-05-29)
Earlier synchrotron photoionization mass spectrometry experiments suggested a prominent ring-opening channel in the OH-initiated oxidation of cyclohexene, based on comparison of product photoionization spectra with calculated spectra of possible isomers. The present work re-examines the OH + cyclohexene reaction, measuring
Oxidative decarboxylation of benzilic acid by a biomimetic iron(II) complex: evidence for an iron(IV)-oxo-hydroxo oxidant from O2.
Sayantan Paria et al.
Angewandte Chemie (International ed. in English), 50(47), 11129-11132 (2011-10-01)
Sylvain Dalençon et al.
The Journal of organic chemistry, 76(19), 8059-8063 (2011-08-26)
The asymmetric synthesis of novel cyclohexene nucleoside analogues 12 and 15 is described. An enantiospecific Diels-Alder reaction between (E,E)-diene 2 and (+)-5-(d-mentyloxy)-2(5H)-furanone 3 provided the cycloadduct isomer 4. Three additional steps yielded amine 8 allowing the constructions of the thymine
Emanuele Monza et al.
The journal of physical chemistry. A, 115(45), 12864-12878 (2011-07-19)
The source function (SF) introduced in late 90s by Bader and Gatti quantifies the influence of each atom in a system in determining the amount of electron density at a given point, regardless of the atom's remote or close location
Oleg Y Lyakin et al.
Inorganic chemistry, 50(12), 5526-5538 (2011-05-24)
Complexes [(BPMEN)Fe(II)(CH(3)CN)(2)](ClO(4))(2) (1, BPMEN = N,N'-dimethyl-N,N'-bis(2-pyridylmethyl)-1,2-diaminoethane) and [(TPA)Fe(II)(CH(3)CN)(2)](ClO(4))(2) (2, TPA = tris(2-pyridylmethyl)amine) are among the best nonheme iron-based catalysts for bioinspired oxidation of hydrocarbons. Using EPR and (1)H and (2)H NMR spectroscopy, the iron-oxygen intermediates formed in the catalyst systems
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