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MilliporeSigma

228796

Sigma-Aldrich

3-Thiopheneethanol

99%

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C6H8OS
Número de CAS:
Peso molecular:
128.19
Beilstein/REAXYS Number:
107080
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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.)

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

10 - Combustible liquids

wgk_germany

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)


Certificados de análisis (COA)

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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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