37879
甘菊蓝
analytical standard
别名:
奥甘菊环
等级
analytical standard
保质期
limited shelf life, expiry date on the label
技术
HPLC: suitable
gas chromatography (GC): suitable
沸点
242 °C (lit.)
mp
98-100 °C (lit.)
应用
environmental
包装形式
neat
SMILES字符串
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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应用
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
其他说明
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.
危险声明
预防措施声明
危险分类
Aquatic Chronic 2
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
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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