A97203
Azulene
99%
Synonym(s):
Bicyclo[5.3.0]decapentaene
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100 MG
MXP 1,770.00
1 G
MXP 4,835.00
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100 MG
MXP 1,770.00
1 G
MXP 4,835.00
About This Item
Empirical Formula (Hill Notation):
C10H8
CAS Number:
Molecular Weight:
128.17
Beilstein:
969517
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
form:
crystals
Assay:
99%
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Quality Level
Assay
99%
form
crystals
bp
242 °C (lit.)
mp
98-100 °C (lit.)
SMILES string
c1ccc2cccc2cc1
InChI
1S/C10H8/c1-2-5-9-7-4-8-10(9)6-3-1/h1-8H
InChI key
CUFNKYGDVFVPHO-UHFFFAOYSA-N
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Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Stefan Löber et al.
ChemMedChem, 4(3), 325-328 (2009-02-03)
Blue makes it happen: The non-uniform charge distribution of the blue colored azulene framework is highly suitable for the bioisosteric replacement of bicyclic heteroarene moieties. Showing an analogous binding mode as heterocyclic dopamine D4 receptor-selective lead compounds, the induction of
A F M Mustafizur Rahman et al.
Chemical communications (Cambridge, England), (10)(10), 1196-1198 (2008-03-01)
In spite of having small pi-conjugation systems, azulenes show large binding constants (10(4)-10(5)) to C(60) and C(70), which are larger than those of monoporphyrins and alternant aromatic hydrocarbons.
Atsuya Muranaka et al.
Journal of the American Chemical Society, 132(23), 7844-7845 (2010-05-27)
Azulenocyanine, having four azulene units fused to a tetraazaporphyrin skeleton, is a structural isomer of naphthalocyanine. We synthesized the first example of an azulenocyanine from 1,3-di-tert-butyl-5,6-dicyanoazulene. The macrocycle exhibits broad absorption over the visible and near-IR regions far beyond 1000
Hiromi Mitsuhashi et al.
European journal of pharmacology, 551(1-3), 152-155 (2006-10-19)
Oral ulcerative mucositis is a common and painful toxicity associated with chemotherapy for cancer. Current treatment for chemotherapy-induced oral mucositis is largely palliative, and no adequate treatment with conclusive evidence exists. The purpose of this study was to evaluate the
Chih-Hung Chen et al.
Bioorganic & medicinal chemistry letters, 20(20), 6129-6132 (2010-09-14)
A series of azulene-based derivatives were synthesized as potent inhibitors for receptor tyrosine kinases such as FMS-like tyrosine kinase 3 (FLT-3). Systematic side chain modification of prototype 1a was carried out through SAR studies. Analogue 22 was identified from this
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