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Merck
CN

37879

Supelco

Azulene

analytical standard

Synonym(s):

Bicyclo[5.3.0]decapentaene

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About This Item

Empirical Formula (Hill Notation):
C10H8
CAS Number:
275-51-4
Molecular Weight:
128.17
Beilstein:
969517
EC Number:
205-993-6
MDL number:
MFCD00003810
UNSPSC Code:
41116107
PubChem Substance ID:
329755704
NACRES:
NA.24

Key Documents

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grade

analytical standard

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

242 °C (lit.)

mp

98-100 °C (lit.)

application(s)

environmental

format

neat

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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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictograms

Environment
GHS09

Hazard Statements

H411

Precautionary Statements

P273 - P391 - P501

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCD7841
BCCB7702
BCBW5128

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Karol Michalak et al.
The Journal of organic chemistry, 76(16), 6906-6911 (2011-07-07)
An efficient synthesis of the key building block for 17-epi-calctriol from the Hajos-Parrish dione involving a sequence of diastereoselective transformation of the azulene core and the side-chain construction is presented.
Yasuyuki Hirama et al.
Bioorganic & medicinal chemistry, 19(1), 352-358 (2010-12-07)
The synthesis and thermal stability of oligodeoxynucleotides (ODNs) containing 4-amino-2,3,5,6-tetraazabenzo[cd]azulen-7-one nucleosides 5 (BaO(N)) with the aim of developing new base pairing motif is described. The tricyclic nucleoside 5 was prepared starting with the 7-deaza-7-iodopurine derivative 1 via a palladium catalyzed
B Benedek et al.
Die Pharmazie, 63(1), 23-26 (2008-02-15)
Yarrow (Achillea millefolium L. s.l.) is traditionally used against inflammatory and spasmodic gastrointestinal complaints, hepato-biliary disorders, as an appetite enhancing drug, against skin inflammations and for wound healing due to its antiphlogistic, choleretic and spasmolytic properties. The main pharmacologically active
Jun-ichiro Kitai et al.
The Journal of organic chemistry, 77(7), 3270-3276 (2012-03-14)
Diarylethene derivatives incorporating an azulene ring at the ethene moiety were synthesized. One derivative having thiazole rings showed the expected coloration reaction by excitation at 313 nm (to a higher singlet state) but not when excited at 635 nm (S(0)
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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