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129801

Sigma-Aldrich

1-Methyl-1-cyclohexene

97%

Synonym(s):

2,3,4,5-Tetrahydrotoluene

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About This Item

Linear Formula:
C6H9CH3
CAS Number:
Molecular Weight:
96.17
Beilstein:
1304483
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

liquid

refractive index

n20/D 1.45 (lit.)

bp

110-111 °C (lit.)

density

0.811 g/mL at 20 °C (lit.)

SMILES string

CC1=CCCCC1

InChI

1S/C7H12/c1-7-5-3-2-4-6-7/h5H,2-4,6H2,1H3

InChI key

CTMHWPIWNRWQEG-UHFFFAOYSA-N

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General description

1-Methyl-1-cyclohexene (2,3,4,5-Tetrahydrotoluene) is a sterically hindered, unactivated alkene.

Application

1-Methyl-1-cyclohexene (2,3,4,5-Tetrahydrotoluene) was used to study the secondary organic aerosol (SOA) yields from the ozonolysis of cycloalkenes.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

24.8 °F - closed cup

Flash Point(C)

-4 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Renyuan Pony Yu et al.
Journal of the American Chemical Society, 135(35), 13168-13184 (2013-08-24)
The bis(arylimidazol-2-ylidene)pyridine cobalt methyl complex, ((iPr)CNC)CoCH3, was evaluated for the catalytic hydrogenation of alkenes. At 22 °C and 4 atm of H2 pressure, ((iPr)CNC)CoCH3 is an effective precatalyst for the hydrogenation of sterically hindered, unactivated alkenes such as trans-methylstilbene, 1-methyl-1-cyclohexene
M D Keywood et al.
Environmental science & technology, 38(15), 4157-4164 (2004-09-09)
The secondary organic aerosol (SOA) yields from the laboratory chamber ozonolysis of a series of cycloalkenes and related compounds are reported. The aim of this work is to investigate the effect of the structure of the hydrocarbon parent molecule on
Tobias Trapp et al.
Journal of agricultural and food chemistry, 67(49), 13400-13411 (2019-03-01)
The white-rot fungus Pleurotus sapidus (PSA) biosynthesizes the bicyclic monoterpenoids 3,6-dimethyl-2,3,3a,4,5,7a-hexahydrobenzofuran (dill ether) (1) and 3,6-dimethyl-3a,4,5,7a-tetrahydro-1-benzofuran-2(3H)-one (wine lactone) (2). Submerged cultures grown in different media were analyzed by gas chromatography-mass spectrometry. The stereochemistry of the formed isomers was elucidated by

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