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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
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)
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
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
Allergic contact cheilitis to guaiazulene.
G Angelini et al.
Contact dermatitis, 10(5), 311-311 (1984-05-01)
An Azulene Dimer as a Near-Infrared Quencher.
Pham W, et al.
Angewandte Chemie (International Edition in English), 41(19), 3659-3662 (2002)
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