T89702
环庚三烯酚酮
98%
别名:
2-羟基-2,4,6-环庚三烯-1-酮
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关于此项目
经验公式（希尔记法）:
C7H6O2
化学文摘社编号:
分子量:
122.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-577-2
Beilstein/REAXYS Number:
1904978
MDL number:
产品名称
环庚三烯酚酮, 98%
InChI
1S/C7H6O2/c8-6-4-2-1-3-5-7(6)9/h1-5H,(H,8,9)
InChI key
MDYOLVRUBBJPFM-UHFFFAOYSA-N
SMILES string
OC1=CC=CC=CC1=O
assay
98%
bp
80-84 °C/0.1 mmHg (lit.)
mp
50-52 °C (lit.)
storage temp.
2-8°C
Quality Level
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Application
环庚三烯酚酮是对还原糖敏感的试剂。它也是一种有机螯合剂，可与三价镧系离子（Eu3+、Gd3+和Tb3+）形成络合物。
还可用作：
还可用作：
- 合成薁衍生物前体，如合成2-甲基薁-1-羧酸甲酯。
- 试剂，制备Ga（III）和In（III）的稠合杂环 和络合物。
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
233.6 °F - closed cup
flash_point_c
112 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Structural characterization of two lipophilic tris(tropolonato) gallium(III) and indium(III) complexes of radiopharmaceutical interest
F.Nepveu and F.JasanadaL.Walz
Inorgorganica Chimica Acta, 211, 141-141 (1993)
Spectroscopy and non-radiative processes in Gd3+, Eu3+ and Tb3+ tropolonates.
Santos BS, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 54(13), 2237-2245 (1998)
Trends Heterocycl. Chem., 1, 137-137 (1990)
Jinbing Liu et al.
European journal of medicinal chemistry, 44(4), 1773-1778 (2008-06-06)
A series of alkylidenethiosemicarbazide compounds were synthesized and their inhibitory effects on the diphenolase activity of mushroom tyrosinase were evaluated. The results showed that most of the synthesized compounds exhibited significant inhibitory activities. Especially, compound 1f was found to be
Jessica L Fullagar et al.
Chemical communications (Cambridge, England), 49(31), 3197-3199 (2013-03-14)
Tropolone emerged from the screening of a chelator fragment library (CFL) as an inhibitor of the Zn(2+)-dependent virulence factor, Pseudomonas aeruginosa elastase (LasB). Based on this initial hit, a series of substituted tropolone-based LasB inhibitors was prepared, and a compound
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