685828
(R)-1-苯基乙醇
97%
别名:
(+)-α-甲基苯甲醇, (+)-α-苯乙醇, (+)-α-苯基乙醇, (+)-1-苯乙醇, (+)-1-苯基乙醇, (+)-sec-苯乙醇
质量水平
方案
97%
表单
liquid
旋光性
[α]22/D +44.0°, c = 5%
折射率
n20/D 1.528
密度
0.9986 g/mL at 25 °C
官能团
hydroxyl
phenyl
SMILES字符串
C[C@@H](O)c1ccccc1
InChI
1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3/t7-/m1/s1
InChI key
WAPNOHKVXSQRPX-SSDOTTSWSA-N
一般描述
( R )-1-苯乙醇可通过乙苯在过氧化酶催化下的对映选择性羟基化制备。
警示用语：
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
185.0 °F - closed cup
闪点(°C)
85 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Peroxygenase-Catalyzed Oxyfunctionalization Reactions Promoted by the Complete Oxidation of Methanol.
Ni Y, et al.
Angewandte Chemie (International Edition in English), 55(2), 798-801 (2016)
Sachiko Sugimoto et al.
Phytochemistry, 108, 189-195 (2014-12-03)
Three aromatic glycosides (1-3), two sulfur and nitrogen-containing compound glucosides (4, 5), and one flavonoid glycoside (6) were isolated from the leaves of Ixora undulata. Their structures were established by extensive 1D, 2D NMR, and HRESIMS experiments, and structure 4
Chromatograms
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