Skip to Content
Merck
All Photos(1)

Documents

108472

Sigma-Aldrich

2,5-Dibromothiophene

95%

Synonym(s):

2,5-dibromo-thiophene

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4H2Br2S
CAS Number:
Molecular Weight:
241.93
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

refractive index

n20/D 1.629 (lit.)

bp

211 °C (lit.)

mp

−6 °C (lit.)

density

2.147 g/mL at 25 °C (lit.)

SMILES string

Brc1ccc(Br)s1

InChI

1S/C4H2Br2S/c5-3-1-2-4(6)7-3/h1-2H

InChI key

KBVDUUXRXJTAJC-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

2,5-Dibromothiophene polymerizes by debromination with magnesium catalyzed by nickel compounds to form poly(2,5- thienylene) .

Application

2,5-Dibromothiophene was used as starting reagent for the synthesis of α,α′-didecylquater-, -quinque- and -sexi-thiophenes. It was used in the preparation of soluble α,ω-diformyl-a-oligothiophenes.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

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)

210.2 °F - closed cup

Flash Point(C)

99 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Synthesis and thermal behaviour of α, α'-didecyloligothiophenes.
Ponomarenko S and Kirchmeyer S.
Journal of Materials Chemistry, 13(2), 197-202 (2003)
Preparation of thermostable and electric-conducting poly (2, 5-thienylene).
Yamamoto T, et al.
Journal of Polymer Science - Part C: Polymer Letters, 18(1), 9-12 (1980)
Synthesis and characterization of 3−hexyl multi−substituted α, ω−diformyl−α−oligothiophenes (n= 3, 6, 8).
Olinga T, et al.
Macromolecular Chemistry and Physics, 198(4), 1091-1107 (1997)
Minami Kato et al.
ChemSusChem, 13(9), 2379-2385 (2020-02-11)
Many types of batteries have been proposed as next-generation energy-storage systems. One candidate is a rocking-chair-type "molecular ion battery" in which a molecular ion, instead of Li+ , works as a charge carrier. Previously, we reported a viologen-type derivative as

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service