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332399

Sigma-Aldrich

3-Thiophenemethanol

98%

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About This Item

Fórmula empírica (notación de Hill):
C5H6OS
Número de CAS:
71637-34-8
Peso molecular:
114.17
EC Number:
275-741-8
MDL number:
MFCD00014534
UNSPSC Code:
12352100
PubChem Substance ID:
24859892
NACRES:
NA.22

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

SMILES string

OCc1ccsc1

InChI

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

InChI key

BOWIFWCBNWWZOG-UHFFFAOYSA-N

General description

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

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.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

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

Certificados de análisis (COA)

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A comparative study of the electrochemistry of 3-thiophenemethanol and 3-methylthiophene.
Pohjakallio M and Sundholm G.
Synthetic Metals, 55(2), 1590-1595 (1993)
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)
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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