232777
2-苯硫基乙醇
99%
别名:
2-羟乙基苯硫醚
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关于此项目
线性分子式:
C6H5SCH2CH2OH
化学文摘社编号:
分子量:
154.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-828-9
Beilstein/REAXYS Number:
1860057
MDL number:
产品名称
2-苯硫基乙醇, 99%
form
liquid
InChI key
KWWZHCSQVRVQGF-UHFFFAOYSA-N
InChI
1S/C8H10OS/c9-6-7-10-8-4-2-1-3-5-8/h1-5,9H,6-7H2
SMILES string
OCCSc1ccccc1
assay
99%
refractive index
n20/D 1.592 (lit.)
bp
115-116 °C/2 mmHg (lit.)
density
1.143 g/mL at 25 °C (lit.)
functional group
hydroxyl
thioether
Quality Level
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Application
2-(Phenylthio)ethanol has been used:
- in the synthesis of indole, benzofuran and benzothiophene
- for temporary masking of the thymine residue during the synthesis of sugar modified thymidine derivatives
- in the preparation of 4-[2-(phenylthio)ethoxy]phthalonitrile
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
新产品
此项目有
Synthesis of indole, benzofuran and benzothiophene by reaction of 2-anilinoethanol, 2-phenoxyethanol and 2-(phenylthio) ethanol on AlPO4 and Pd/AlPO4 catalysts.
Afxantidis J, et al.
J. Mol. Catal. A: Chem., 102(1), 49-58 (1995)
Synthesis, characterization and electrochemistry of a new organosoluble metal-free and metallophthalocyanines.
Biyiklioglu Z, et al.
Polyhedron, 27(6), 1707-1713 (2008)
2-(Phenylthio) ethyl as a novel two-stage base protecting group for thymidine analogues.
D'Onofrio J, et al.
Synlett, 2006(06), 845-848 null
Xichang Dong et al.
Science (New York, N.Y.), 371(6528), 507-514 (2021-01-30)
Vicinal dibromides and dichlorides are important commodity chemicals and indispensable synthetic intermediates in modern chemistry that are traditionally synthesized using hazardous elemental chlorine and bromine. Meanwhile, the environmental persistence of halogenated pollutants necessitates improved approaches to accelerate their remediation. Here
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