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质量水平
方案
98%
沸点
267 °C (lit.)
mp
71-73 °C (lit.)
SMILES字符串
Cc1ccc2cccc(O)c2n1
InChI
1S/C10H9NO/c1-7-5-6-8-3-2-4-9(12)10(8)11-7/h2-6,12H,1H3
InChI key
NBYLBWHHTUWMER-UHFFFAOYSA-N
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一般描述
2-Methyl-8-quinolinol is a methyl substituted quinolinol derivative that shows fungicidal property. It can also undergo complexation with transition metal complexes.
应用
2-Methyl-8-quinolinol (HqMe) may be used as a ligand for preparing bis (2-methyl-8-quinolinolato) aluminum(III)-μ-oxo-bis (2-methyl-8-quinolinolato ) aluminum (III). It may also be used in the preparation of a scandium 2-methyl-8-quinolinolate complex [Sc(qMe)4(H)].
警示用语：
Warning
危险声明
预防措施声明
危险分类
Aquatic Acute 1 - Aquatic Chronic 1
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
282.2 °F - closed cup
闪点(°C)
139 °C - closed cup
个人防护装备
Eyeshields, Gloves
Monika Krawczyk et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-17)
One of the main factors limiting the effectiveness of many drugs is the difficulty of their delivery to their target site in the cell and achieving the desired therapeutic dose. Moreover, the accumulation of the drug in healthy tissue can
J Thomas Leonard et al.
European journal of medicinal chemistry, 43(1), 81-92 (2007-04-25)
HIV-1 integrase inhibitory activity data of styrylquinoline derivatives have been subjected to 3D-QSAR study by molecular shape analysis (MSA) technique using Cerius(2) version 4.8 software (Accelrys). For the selection of test set compounds, initially a QSAR analysis was done based
Jakub Wantulok et al.
Molecules (Basel, Switzerland), 25(9) (2020-05-02)
A new approach to the synthesis of selected quinolinecarbaldehydes with carbonyl groups located at C5 and/or in C7 positions is presented in this paper in conjunction with spectroscopic characterization of the products. The classical Reimer-Tiemann, Vilsmeier-Haack and Duff aldehyde synthesis
New type of arrangement of rare-earth quinolinolate. Molecular structure of scandium 2-methyl-8-quinolinolate.
Katkova MA, et al.
Inorgorganica Chimica Acta, 362(4), 1393-1395 (2009)
Antifungal activity of 5-,7-, and 5,7-substituted 2-methyl-8-quinolinols.
Gershon H, et al.
Antimicrobial Agents and Chemotherapy, 1(5), 373-375 (1972)
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