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Merck
CN

228796

3-Thiopheneethanol

99%

Synonym(s):

2-(3-Thienyl)ethanol, 3-(2-Hydroxyethyl)thiophene

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About This Item

Empirical Formula (Hill Notation):
C6H8OS
CAS Number:
13781-67-4
Molecular Weight:
128.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24853712
EC Number:
237-434-7
Beilstein/REAXYS Number:
107080
MDL number:
MFCD00009766

Key Documents

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Product Name

3-Thiopheneethanol, 99%

InChI key

YYPNNBPPDFTQFX-UHFFFAOYSA-N

InChI

1S/C6H8OS/c7-3-1-6-2-4-8-5-6/h2,4-5,7H,1,3H2

SMILES string

OCCc1ccsc1

assay

99%

form

liquid

refractive index

n20/D 1.552 (lit.)

bp

110-111 °C/14 mmHg (lit.)

density

1.144 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

100

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Application

3-Thiopheneethanol [3-(2-hydroxyethyl)thiophene] was used in the synthesis of various ether and ester derivatives such as 3-(2-(benzyloxy)ethyl)thiophene, 3-[2-((triphenylmethyl)oxy)ethyl]thiophene, 3-[2-((trimethylsilyl)oxy)ethyl]thiophene, 3-[2-((dimethyl-tert-butylsilyl)oxy)ethyl]thiophene, 3-(2-acetoxyethyl)thiophene and 3-(2-(benzoyloxy)ethyl)thiophene.

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

197.6 °F - closed cup

flash_point_c

92 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000224101
0000224073
0000224073
0000224101
0000133806

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Reactive groups on polymer-covered electrodes. 5. Synthesis and cyclovoltammetric analysis of 3-substituted thiophene derivatives.
Macromolecules, 30(24), 7419-7426 (1997)
Consuelo Ripoll et al.
Pharmaceutics, 13(2) (2021-03-07)
Recently, it was proposed that the thiophene ring is capable of promoting mitochondrial accumulation when linked to fluorescent markers. As a noncharged group, thiophene presents several advantages from a synthetic point of view, making it easier to incorporate such a
Yuwei Hao et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 19(16), 2046-2051 (2018-03-25)
Highly efficient cell capture and release with low background are urgently required for early diagnosis of diseases such as cancer. Herein, we report an electrochemical responsive superhydrophilic surface exhibiting specific cell capture and release with high yields and extremely low

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