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232777

2-苯硫基乙醇

Name: 2-苯硫基乙醇
Brand: ALDRICH

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:

699-12-7

分子量:

154.23

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24853928

EC Number:

211-828-9

Beilstein/REAXYS Number:

1860057

MDL number:

MFCD00002905

Assay:

99%

Form:

liquid

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属性

Quality Level

100

assay

99%

form

liquid

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

SMILES string

OCCSc1ccccc1

InChI

1S/C8H10OS/c9-6-7-10-8-4-2-1-3-5-8/h1-5,9H,6-7H2

InChI key

KWWZHCSQVRVQGF-UHFFFAOYSA-N

说明

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

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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

Synthesis, characterization and electrochemistry of a new organosoluble metal-free and metallophthalocyanines.

Biyiklioglu Z, et al.

Polyhedron, 27(6), 1707-1713 (2008)

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)

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货号	GTIN
232777-50G	04061838783721