所有图片(1)
About This Item
线性分子式:
C6H5CH(OCH3)CH2OH
CAS号:
分子量:
152.19
MDL编号:
UNSPSC代码:
12352112
PubChem化学物质编号:
NACRES:
NA.22
方案
98%
表单
liquid
旋光性
[α]19/D +133°, c = 1 in acetone
光学纯度
ee: 99% (GLC)
折射率
n20/D 1.52 (lit.)
沸点
65 °C/0.1 mmHg (lit.)
密度
1.054 g/mL at 25 °C (lit.)
SMILES字符串
CO[C@H](CO)c1ccccc1
InChI
1S/C9H12O2/c1-11-9(7-10)8-5-3-2-4-6-8/h2-6,9-10H,7H2,1H3/t9-/m1/s1
InChI key
JDTUPLBMGDDPJS-SECBINFHSA-N
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应用
(S)-(+)-2-Methoxy-2-phenylethanol can be used:
- As a starting material for the synthesis of N-substituted 6,7-benzomorphan based opioid receptor agonists.
- As a ligand in the preparation of organolanthanoid complexes.
- As starting material for the synthesis of N-acetyl-O-((2S)-2-methoxy-2-phenylethyl)-L-serine, a serine proteases inhibitor.
警示用语:
Warning
危险分类
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
208.4 °F - closed cup
闪点(°C)
98 °C - closed cup
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Probing enzyme stereospecificity. Evaluation of β-alkoxy-α-amino acids with two stereocenters as inhibitors of serine proteases
Lee T and Jones JB
Tetrahedron, 51(27), 7331-7346 (1995)
Solid-state and solution structures of several new [LnCp′ 2 (OR)] 2 complexes (Ln= Pr, Yb) with chiral, oxygen-functionalized mu-alkoxide ligands
Steudel A, et al.
Journal of Organometallic Chemistry, 570(1), 89-96 (1998)
(2S)-N-2-methoxy-2-phenylethyl-6,7-benzomorphan compound (2S-LP2): Discovery of a biased mu/delta opioid receptor agonist
Pasquinucci L, et al.
European Journal of Medicinal Chemistry, 168, 189-198 (2019)
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