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Merck
CN

332399

3-Thiophenemethanol

98%

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About This Item

Empirical Formula (Hill Notation):
C5H6OS
CAS Number:
Molecular Weight:
114.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
275-741-8
MDL number:
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Product Name

3-Thiophenemethanol, 98%

InChI key

BOWIFWCBNWWZOG-UHFFFAOYSA-N

InChI

1S/C5H6OS/c6-3-5-1-2-7-4-5/h1-2,4,6H,3H2

SMILES string

OCc1ccsc1

assay

98%

form

liquid

refractive index

n20/D 1.564 (lit.)

bp

86-88 °C/10 mmHg (lit.)

density

1.211 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

Application

3-Thiophenemethanol was used in the preparation of 3-substituted thiophene conducting copolymers which has potential applications in electrochromic displays. It was also used in the synthesis of 4-(thiophene-3-ylmethoxy)phthalonitrile.

General description

Comparision of electrochemical polymerization properties of 3-thiophenemethanol and 3-methylthiophene has been reported.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

213.8 °F - closed cup

flash_point_c

101 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Synthesis, molecular conformation, vibrational, electronic transition, and chemical shift assignments of 4-(thiophene-3-ylmethoxy) phthalonitrile: a combined experimental and theoretical analysis.
Coruh A, et al.
Structural Chemistry, 22(1), 45-56 (2011)
A comparative study of the electrochemistry of 3-thiophenemethanol and 3-methylthiophene.
Pohjakallio M and Sundholm G.
Synthetic Metals, 55(2), 1590-1595 (1993)
Electrochemical polymerization and characterization of new copolymers of 3-substituted thiophenes.
Alves MRA, et al.
Synthetic Metals, 160(1), 22-27 (2010)
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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