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Merck
CN

44028

Cyclohexene

analytical standard, ≥99.5% (GC)

Synonym(s):

Tetrahydrobenzene

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About This Item

Empirical Formula (Hill Notation):
C6H10
CAS Number:
110-83-8
Molecular Weight:
82.14
NACRES:
NA.24
PubChem Substance ID:
329756445
EC Number:
203-807-8
Beilstein/REAXYS Number:
906737
MDL number:
MFCD00001539
UNSPSC Code:
12141716

Key Documents

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Product Name

Cyclohexene, analytical standard, ≥99.5% (GC)

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

refractive index

n20/D 1.446 (lit.)
n20/D 1.446

bp

83 °C (lit.)

mp

−104 °C (lit.)

density

0.811 g/mL at 25 °C (lit.)

application(s)

environmental
petroleum

format

neat

Quality Level

100

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Asp. Tox. 1 - Flam. Liq. 2

Storage Class

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

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCL7514
BCCK6886
BCCJ4837
BCCG8149
BCCF6170

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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
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)
Qingshan Zhao et al.
Nanoscale, 5(3), 882-885 (2012-12-15)
Rhodium complexes can be homogeneously immobilized on functionalized graphene oxide through coordination interaction. The obtained catalyst can be readily recycled and shows enhanced activity in the catalytic hydrogenation of cyclohexene.
El Sayed H El Ashry et al.
Bioorganic & medicinal chemistry, 20(9), 3000-3008 (2012-04-07)
The immunomodulating properties of functionalized [2-(arylamino)-4,4-dimethyl-6-oxo-cyclohex-1-ene] carbodithioates and 6,6-dimethyl-4-(2-(propan-2-ylidene)hydrazinyl)-6,7-dihydro-2H-indazole-3(5H)-thione compounds have been investigated. Four of them, 13, 18, 19 and 20 inhibited PBMC proliferation induced by phytohemagglutinin (PHA) in a dose dependent manner with an IC(50) of ≤ 20 μM.
Amit Aggarwal et al.
Macromolecular rapid communications, 33(14), 1220-1226 (2012-04-21)
Self-organized organic nanoparticles (ONP) are adaptive to the environmental reaction conditions. ONP of fluorous alkyl iron(III) porphyrin catalytically oxidize cyclohexene to the allylic oxidation products. In contrast, the solvated metalloporphyrin yields both allylic oxidation and epoxidation products. The ONP system
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