5-甲基水杨醛

5-甲基水杨醛结构式
5-甲基水杨醛结构式
品牌特惠专场
常用名 5-甲基水杨醛 英文名 2-Hydroxy-5-methylbenzaldehyde
CAS号 613-84-3 分子量 136.148
密度 1.2±0.1 g/cm3 沸点 217.5±0.0 °C at 760 mmHg
分子式 C8H8O2 熔点 54-57 °C(lit.)
MSDS 中文版 美版 闪点 85.1±14.4 °C
符号 GHS07
GHS07
信号词 Warning

Mixed ligand copper(II) complexes of 1,10-phenanthroline with tridentate phenolate/pyridyl/(benz)imidazolyl Schiff base ligands: covalent vs non-covalent DNA binding, DNA cleavage and cytotoxicity.

J. Inorg. Biochem. 140 , 255-68, (2014)

A series of copper(II) complexes of the types [Cu(L)(phen)](ClO4) 1-2, where HL is a tridentate ligand with two nitrogen and one oxygen donor atoms (2NO) such as 2-(2-(1H-benzimidazol-2-yl)ethyliminomethyl)phenol (HL1) and 2-(2-(1H-benzimidazol-2-yl)ethyl-imi...

Antifungal activity of redox-active benzaldehydes that target cellular antioxidation.

Ann. Clin. Microbiol. Antimicrob. 10 , 23, (2011)

Disruption of cellular antioxidation systems should be an effective method for control of fungal pathogens. Such disruption can be achieved with redox-active compounds. Natural phenolic compounds can serve as potent redox cyclers that inhibit microbial growth...

Nanoplatforms attached Schiff bases by condensation method; Investigation of glucose oxidase enzyme as biocatalysts.

Artif. Cells. Nanomed. Biotechnol. 43 , 224-9, (2015)

We report a easy approach for the immobilization of glucose oxidase enzyme (GOx) on nanoparticles. Nanoparticles-modified polystyrene-ANH2 (PSA) with some salicylaldehyde derivatives were synthesized by means of condensation and investigated the enzymatic pro...

Spectroscopy and stereochemistry of the optically active copper (II), cobalt (II) and nickel (II) complexes with Schiff bases N,N'-(1R,2R)-(-)-1, 2-cyclohexylenebis(3-methylbenzylideneiminato) and N,N'-(1R,2R)-(-)-1,2-cyclohexylenebis(5-methylbenzylideneiminato) Szlyk E, et al.

Polyhedron 21(27) , 2711-17, (2002)

Syntheses, structures and electrochemistry of copper (II) salicylaldehyde/tris (3-phenylpyrazolyl) borate complexes as models for the radical copper oxidases. Halcrow MA, et al.

J. Chem. Soc., Dalton Trans. 11 , 1753-1762, (1999)