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Safety Information

733725

Sigma-Aldrich

3,3′-Dibromo-2,2′-bithiophene

97%

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About This Item

Empirical Formula (Hill Notation):
C8H4Br2S2
CAS Number:
51751-44-1
Molecular Weight:
324.06
MDL number:
MFCD00114806
UNSPSC Code:
12352103
PubChem Substance ID:
329764841
NACRES:
NA.23

Assay

97%

form

powder

mp

97-101 °C

SMILES string

Brc1ccsc1-c2sccc2Br

InChI

1S/C8H4Br2S2/c9-5-1-3-11-7(5)8-6(10)2-4-12-8/h1-4H

InChI key

KBRZCEVRNLKHAZ-UHFFFAOYSA-N

Related Categories

Application

3,3′-Dibromo-2,2′-bithiophene can potentially be used in the designing and synthesis of a variety of optoelectronic and electronic devices, which include organic solar cells, thin film transistors, chemical sensors and photovoltaic cells.

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H301,H318

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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.

JAN Code

733725-BULK:
733725-VAR:
733725-5G:
733725-1G:

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Certificates of Analysis (COA)

Lot/Batch Number
BGBC1745V
BGBB9786
MKBK1118V
MKBH8240V
MKBG6655V

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Transistor Paint: Environmentally Stable N-alkyldithienopyrrole and Bithiazole-Based Copolymer Thin-Film Transistors Show Reproducible High Mobilities without Annealing
Liu J, et al.
Advances in Functional Materials, 19(21), 3427-3434 (2009)

Articles

Organic Bioelectronic Materials and Devices for Bridging Biology and Traditional Electronics

Professor Rivnay (Northwestern University, USA) discusses using organic mixed conductors as an alternative to efficiently bridge the ionic world of biology with contemporary microelectronics.

Synthetic Strategy for Large Scale Production of Oligothiophenes

Oligothiophenes are important organic electronic materials which can be produced using synthetic intermediates and Suzuki coupling.

Development of organic semiconductors from highly ordered oligo and polythiophenes

The soaring global demand for energy, coupled with the limited supply of fossil fuels, has increased the need for renewable, low-cost energy sources. Organic electronics have shown great promise for applications in lighting, power, and circuitry, with rapidly improving performance already surpassing that of amorphous silicon-based counterparts.

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