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经验公式(希尔记法):
C15H18
化学文摘社编号:
分子量:
198.30
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-701-2
Beilstein/REAXYS Number:
1365001
MDL number:
产品名称
愈创奥, 99%
InChI key
FWKQNCXZGNBPFD-UHFFFAOYSA-N
InChI
1S/C15H18/c1-10(2)13-7-5-11(3)14-8-6-12(4)15(14)9-13/h5-10H,1-4H3
SMILES string
CC(C)c1ccc(C)c2ccc(C)c2c1
assay
99%
bp
153 °C/7 mmHg (lit.)
mp
27-29 °C (lit.)
density
0.976 g/mL at 25 °C (lit.)
Quality Level
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Application
愈创木烯可用作合成
- 氮杂戊烯基染料分子(如 3-(7-异丙基-1,4-二甲基氮杂戊烯-3-基)-2-氰基丙烯酸和 5-(7-异丙基-1,4-二甲基氮杂戊烯-3-基)-2-氰基戊烯-2,4-二烯酸)的起始物料。
- Stilbazulenyl nitrone,第二代氮烯基硝酮,可用作断链抗氧化剂。
- 基于双氮杂戊基的近红外荧光猝灭剂。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Y Seo et al.
Journal of natural products, 59(10), 985-986 (1996-10-01)
Three pigments of the guaiazulene class have been isolated from the gorgonian Calicogorgia granulosa. Structures of these compounds have been determined as guaiazulene, 2,2'- diguaiazulenylmethane, and a new compound, 2,2'-biguaiazulenyl, by combined chemical and spectroscopic methods. 2,2'-Biguaiazulenyl exhibited moderate antimicrobial
Stilbazulenyl nitrone (STAZN): a nitronyl-substituted hydrocarbon with the potency of classical phenolic chain-breaking antioxidants.
Becker DA, et al.
Journal of the American Chemical Society, 124(17), 4678-4684 (2002)
Jessica Fiori et al.
Rapid communications in mass spectrometry : RCM, 22(17), 2698-2706 (2008-08-06)
The photostability of guaiazulene (1,4-dimethyl-7-isopropylazulene; GA), a natural azulenic compound used in cosmetic and health-care products, as well as in pharmaceutical preparations, was investigated in solution (methanol, ethanol, acetonitrile), by different techniques: gas chromatography/mass spectrometry (GC/MS) and high-performance liquid chromatography
E Dovolou et al.
Reproduction in domestic animals = Zuchthygiene, 46(5), 862-869 (2011-02-18)
Reactive oxygen species (ROS) are between the major contributors for the reduced rate of in vitro bovine embryo production. It is believed that they can cause abnormal meiosis of oocytes, developmental arrest or cell death of embryos. Reports on the
Determination of the ophthalmic drug guaiazulene by high-performance liquid chromatography.
E Vidal-Ollivier et al.
Journal of chromatography, 463(1), 227-228 (1989-01-20)
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