Azulene - CAS 275-51-4

Catalog	Size	Price	Stock	Quantity
BB019608	1 g	$298	In stock

Add to cart Inquiry

Technical Data

IUPAC Name:	azulene
Description:	Azulene is used in the preparation of dyes.
Molecular Weight:	128.17
Molecular Formula:	C10H8
Canonical SMILES:	C1=CC=C2C=CC=C2C=C1
InChI:	InChI=1S/C10H8/c1-2-5-9-7-4-8-10(9)6-3-1/h1-8H
InChI Key:	CUFNKYGDVFVPHO-UHFFFAOYSA-N
Boiling Point:	242 °C
Melting Point:	99-101 °C
Flash Point:	241-243°C
Purity:	> 98 %
Density:	1.037 g/cm³
Solubility:	water, 50.22 mg/L @ 25 °C (est)
Appearance:	Dark blue to purple crystalline powder
Storage:	Powder: 3 years -20°C In solvent: 2 years -80°C
MDL:	MFCD00003810
LogP:	2.79140
Refractive Index:	1.632
Stability:	Stable. Combustible. Incompatible with strong oxidizing agents.
Vapor Pressure:	0.2±0.2 mmHg at 25°C

Publication Number	Title	Priority Date
CN-113480479-A	Urea multi-target tyrosine kinase inhibitor and medical application thereof	20210812
CN-113318167-A	Traditional Chinese medicine composition for treating rheumatoid arthritis	20210707
RU-2021118093-A	The method of obtaining the author's relaxing, sedative, anxiolytic, antidepressant biologically active pharmacological composition with the composition: - dihydroquercetin; -kempferol; -chlorophylls; -azulene; -guayazulene; -isovitexin; -borneol; -alfa pinene; -limonene; -alpha, -beta fellandren; -sabinol; -myrcene; -betulin, -pectins from plant raw materials of foliage of common juniper Juniperus communist L, Siberian larch Paris Sibrica, drooping birch Betula pendula, chamomile Matricaria chlamomilla, common beet root crops Beta vulgaris in a chemical percolator reactor on specially activated extractants	20210621
CN-113144150-A	Traditional Chinese medicine for reducing blood fat and preparation method thereof	20210616
CN-113201422-A	Preparation method of multi-sugar alcohol mineral rock facial soap	20210607

PMID	Publication Date	Title	Journal
23099096	20121201	Novel azulene derivatives for the treatment of erectile dysfunction	Bioorganic & medicinal chemistry letters
23025237	20121015	Synthesis and electrochemistry of organometallic cobaltadithiaazulenes	Inorganic chemistry
22976540	20121003	Synthesis of push-pull chromophores by the sequential [2 + 2] cycloaddition of 1-azulenylbutadiynes with tetracyanoethylene and tetrathiafulvalene	Organic & biomolecular chemistry
22898878	20121001	Probing the interplay between factors determining reaction rates on silica gel using termolecular systems	Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology
22616814	20120615	Experimental and theoretical analyses of azulene synthesis from tropones and active methylene compounds: reaction of 2-methoxytropone and malononitrile	The Journal of organic chemistry

Complexity:	94.6
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	128.062607
Formal Charge:	0
Heavy Atom Count:	10
Hydrogen Bond Acceptor Count:	0
Hydrogen Bond Donor Count:	0
Isotope Atom Count:	0
Monoisotopic Mass:	128.062600255
Rotatable Bond Count:	0
Topological Polar Surface Area:	0
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	3.2