160687
2-Cyclohepten-1-one
80%, technical grade
Synonym(s):
2-Cycloheptenone, Tropilene
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About This Item
Linear Formula:
C7H10(=O)
CAS Number:
Molecular Weight:
110.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
214-334-1
MDL number:
Assay:
80%
Form:
liquid
grade
technical grade
Quality Level
assay
80%
form
liquid
refractive index
n20/D 1.494 (lit.)
density
0.988 g/mL at 25 °C (lit.)
functional group
ketone
storage temp.
2-8°C
SMILES string
O=C1CCCCC=C1
InChI
1S/C7H10O/c8-7-5-3-1-2-4-6-7/h3,5H,1-2,4,6H2
InChI key
WZCRDVTWUYLPTR-UHFFFAOYSA-N
General description
2-Cyclohepten-1-one is an α,β-enone and its regioselective reaction with allyl indium reagent in the presence of TMSCl has been reported. It reacts with Bu2Zn in the presence of catalytic amounts of Cu(OTf)2 and CH2-bridged azolium salts to give (S)-3-butylcycloheptanone.
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T Masukawa et al.
Life sciences, 44(6), 417-424 (1989-01-01)
To search for a technique to deplete reduced glutathione (GSH) in brain, the influence of various types of compounds on brain GSH levels was investigated in mice. Of the compounds tested, cyclohexene-1-one, cycloheptene-1-one and diethyl maleate were shown to be
G Benzi et al.
Neurobiology of aging, 12(3), 227-231 (1991-05-01)
A severe age-dependent depletion of reduced glutathione (GSH) occurs in rat forebrain at 1-3 h from intraperitoneal injection of the electrophilic agents cyclohexene-1-one and cycloheptene-1-one. Chronic pretreatment with central dopamine agonists (i.e., ergot alkaloids; particularly, dihydroergocriptine) partially counteracts the GSH
Kleber Thiago de Oliveira et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 63(3), 709-713 (2005-07-19)
A detailed analysis with total assignment of (1)H and (13)C NMR spectral data for a cycloheptenone derivative, a key intermediate for the synthesis of perhydroazulene terpenoids, is related. These assignments are based on 1D (1)H and (13)C NMR and on