质量水平
检测方案
98%
mp
86-89 °C (lit.)
SMILES字符串
OCC(=O)c1ccccc1
InChI
1S/C8H8O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,9H,6H2
InChI key
ZWVHTXAYIKBMEE-UHFFFAOYSA-N
应用
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。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
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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
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