A97203
Azulene
99%
Sinonimo/i:
Bicyclo[5.3.0]decapentaene
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About This Item
Formula empirica (notazione di Hill):
C10H8
Numero CAS:
Peso molecolare:
128.17
Beilstein:
969517
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
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Saggio
99%
Forma fisica
crystals
P. eboll.
242 °C (lit.)
Punto di fusione
98-100 °C (lit.)
Stringa SMILE
c1ccc2cccc2cc1
InChI
1S/C10H8/c1-2-5-9-7-4-8-10(9)6-3-1/h1-8H
CUFNKYGDVFVPHO-UHFFFAOYSA-N
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Categorie correlate
Confezionamento
Bottomless glass bottle. Contents are inside inserted fused cone.
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Aquatic Chronic 2
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves
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I clienti hanno visto anche
Lorenzo Stella et al.
Chemical communications (Cambridge, England), (39)(39), 4744-4746 (2008-10-03)
We show here that the recently reported surprisingly large association constant (K = 7.6 x 10(4) M(-1)) between azulene and [60]fullerene is due to experimental artifacts, pointing out potential errors in the characterization of association equilibria by fluorescence spectroscopy, and
Aguinaldo Silva Garcez et al.
Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics, 102(4), e93-e98 (2006-09-26)
To investigate the action of a red laser associated with a photosensitizer on the reduction of Enterococcus faecalis in dental root canal in vitro. Thirty prepared teeth with single canals were contaminated. The chemical group was irrigated with 0.5% NaOCl
Stefan Löber et al.
Bioorganic & medicinal chemistry letters, 22(23), 7151-7154 (2012-10-27)
Based on the dopamine D(4) receptor partial agonist FAUC 3019, a series of azulenylmethylpiperazines was synthesized and affinities for the monoaminergic GPCRs including dopamine, serotonin, histamine and α-adrenergic receptor subtypes were determined. Ligand efficacies of the most promising test compounds
Mine Ince et al.
Chemical communications (Cambridge, England), 48(34), 4058-4060 (2012-03-22)
A novel supramolecular electron donor-acceptor hybrid (2·1) and an electron donor-acceptor conjugate (3), both exhibiting a remarkably shifted Q band in the NIR region of the solar spectrum, were prepared. Irradiation of the supramolecular ensemble 2·1 within the visible range
Dawei Zhao et al.
The Journal of chemical physics, 131(18), 184307-184307 (2009-11-18)
The infrared (IR) spectrum of protonated azulene (AzuH(+), C(10)H(9)(+)) has been measured in the fingerprint range (600-1800 cm(-1)) by means of IR multiple photon dissociation (IRMPD) spectroscopy in a Fourier transform ion cyclotron resonance mass spectrometer equipped with an electrospray
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