产品名称
2-羟基苯乙酮, 98%
InChI key
ZWVHTXAYIKBMEE-UHFFFAOYSA-N
InChI
1S/C8H8O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,9H,6H2
SMILES string
OCC(=O)c1ccccc1
assay
98%
mp
86-89 °C (lit.)
functional group
hydroxyl
ketone
phenyl
Quality Level
Application
2-羟基苯乙酮可作为起始材料用于合成：
- 铑(III)催化的不对称转移氢化反应合成对映选择性1R-苯基-1,2-乙二醇。
- 2-羟基苯乙酮N-取代氨基硫脲的铜(II)配合物。
- 2-羟基苯乙酮席夫碱的铬、钼和钌配合物。
- 2-羟基苯乙酮-芳甲酰腙衍生物，用于抑制硝酸溶液中的铜腐蚀。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Chromium, molybdenum and ruthenium complexes of 2-hydroxyacetophenone Schiff bases
Ali SA, et al.
Journal of Coordination Chemistry, 55(10), 1161-1170 (2002)
Mateusz Łużny et al.
Molecules (Basel, Switzerland), 24(17) (2019-09-05)
Biotransformations were performed on eight selected yeast strains, all of which were able to selectively hydrogenate the chalcone derivatives 3-(2"-furyl)- (1) and 3-(2"-thienyl)-1-(2'-hydroxyphenyl)-prop-2-en-1-one (3) into 3-(2"-furyl)- (2) and 3-(2"-thienyl)-1-(2'-hydroxyphenyl)-propan-1-one (4) respectively. The highest efficiency of hydrogenation of the double bond
Synthesis and structural characterization of mixed ligand ? 1-2-hydroxyacetophenone complexes of cobalt (III).
Mondal N, et al.
Polyhedron, 19(28), 2707-2711 (2000)
A stereochemically well-defined rhodium (III) catalyst for asymmetric transfer hydrogenation of ketones
Matharu DS, et al.
Organic Letters, 7(24), 5489-5491 (2005)
Synthetic studies on optically active Schiff-base ligands derived from condensation of 2-hydroxyacetophenone and chiral diamines.
Gao WT and Zheng Z.
Molecules (Basel), 7(7), 511-516 (2002)
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