141720
Cycloheptene
97%
Synonym(s):
(1Z)-Cycloheptene, cis-Cycloheptene
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About This Item
Empirical Formula (Hill Notation):
C7H12
CAS Number:
Molecular Weight:
96.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-060-4
Beilstein/REAXYS Number:
1900884
MDL number:
Assay:
97%
Quality Level
assay
97%
refractive index
n20/D 1.458 (lit.)
bp
112-114.7 °C (lit.)
density
0.824 g/mL at 25 °C (lit.)
SMILES string
C1CCC=CCC1
InChI
1S/C7H12/c1-2-4-6-7-5-3-1/h1-2H,3-7H2
InChI key
ZXIJMRYMVAMXQP-UHFFFAOYSA-N
General description
Kinetics of gas-phase reactions of cycloheptene with NO3 radicals and O3 has been investigated.
Application
Cycloheptene was used in one-pot synthesis of 1,2/3-triols from the allylichydroperoxides catalyzed by zeolite-confined osmium(0) nanoclusters.
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One-pot synthesis of 1, 2/3-triols from the allylic hydroperoxides catalyzed by zeolite-confined osmium (0) nanoclusters.
Goksu H, et al.
J. Mol. Catal. A: Chem., 378, 142-147 (2013)
Sherri A Mason et al.
The journal of physical chemistry. A, 113(19), 5649-5656 (2009-04-24)
Rate constants for the gas-phase reactions of NO(3) radicals and O(3) with a series of C(6)-C(14) 1-alkenes and 2-methyl-1-alkenes have been measured at 296 +/- 2 K and atmospheric pressure of air using relative rate methods. For the NO(3) radical
Alla Zelenyuk et al.
Faraday discussions, 200, 143-164 (2017-06-06)
When secondary organic aerosol (SOA) particles are formed by ozonolysis in the presence of gas-phase polycyclic aromatic hydrocarbons (PAHs), their formation and properties are significantly different from SOA particles formed without PAHs. For all SOA precursors and all PAHs, discussed