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332399

Sigma-Aldrich

3-Thiophenemethanol

98%

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About This Item

Empirical Formula (Hill Notation):
C5H6OS
CAS Number:
71637-34-8
Molecular Weight:
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.)

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

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

213.8 °F - closed cup

Flash Point(C)

101 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

332399-VAR:
332399-25G:
332399-BULK:
332399-5G:

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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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)
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)
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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