A97203
Azulene
99%
Synonyme(s) :
Bicyclo[5.3.0]decapentaene
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About This Item
Produits recommandés
Pureté
99%
Forme
crystals
Point d'ébullition
242 °C (lit.)
Pf
98-100 °C (lit.)
Chaîne SMILES
c1ccc2cccc2cc1
InChI
1S/C10H8/c1-2-5-9-7-4-8-10(9)6-3-1/h1-8H
Clé InChI
CUFNKYGDVFVPHO-UHFFFAOYSA-N
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Catégories apparentées
Conditionnement
Bottomless glass bottle. Contents are inside inserted fused cone.
Mentions de danger
Conseils de prudence
Classification des risques
Aquatic Chronic 2
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves
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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
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
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
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
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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