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141720

Sigma-Aldrich

Cycloheptene

97%

Synonym(s):

(1Z)-Cycloheptene, cis-Cycloheptene

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About This Item

Empirical Formula (Hill Notation):
C7H12
CAS Number:
628-92-2
Molecular Weight:
96.17
Beilstein:
1900884
EC Number:
211-060-4
MDL number:
MFCD00004156
UNSPSC Code:
12352100
PubChem Substance ID:
24848512
NACRES:
NA.22

Quality Level

100

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

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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.

Pictograms

Flame
GHS02

Signal Word

Danger

Hazard Statements

H225

Precautionary Statements

P210

Hazard Classifications

Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

19.4 °F - closed cup

Flash Point(C)

-7 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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

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