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228796

Sigma-Aldrich

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
Beilstein:
107080
EC Number:
237-434-7
MDL number:
MFCD00009766
UNSPSC Code:
12352100
PubChem Substance ID:
24853712
NACRES:
NA.22

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

SMILES string

OCCc1ccsc1

InChI

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

InChI key

YYPNNBPPDFTQFX-UHFFFAOYSA-N

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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 Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

197.6 °F - closed cup

Flash Point(C)

92 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000224101
0000224073
SHBH7753
SHBJ0337
SHBF9669V

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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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