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332399

Sigma-Aldrich

3-Thiophenemethanol

98%

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About This Item

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

Quality Level

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.)

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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

wgk_germany

WGK 3

flash_point_f

213.8 °F

flash_point_c

101 °C

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Electrochemical polymerization and characterization of new copolymers of 3-substituted thiophenes.
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Synthetic Metals, 160(1), 22-27 (2010)
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)
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