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Key Documents

Altri documenti

456373

Sigma-Aldrich

2,5-Dibromo-3-hexylthiophene

97%

Sinonimo/i:

2,5-Dibromo-3-hex-1-ylthiophene

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About This Item

Formula empirica (notazione di Hill):
C10H14Br2S
Numero CAS:
116971-11-0
Peso molecolare:
326.09
Numero MDL:
MFCD00274313
Codice UNSPSC:
12352103
ID PubChem:
24869169
NACRES:
NA.23

Livello qualitativo

100

Saggio

97%

Indice di rifrazione

n20/D 1.557 (lit.)

Densità

1.521 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

CCCCCCc1cc(Br)sc1Br

InChI

1S/C10H14Br2S/c1-2-3-4-5-6-8-7-9(11)13-10(8)12/h7H,2-6H2,1H3
NSYFIAVPXHGRSH-UHFFFAOYSA-N

Categorie correlate

Descrizione generale

2,5-Dibromo-3-hexylthiophene is a 2,5 coupled conductive polymer with conjugated polythiophene based system, which has a controllable band gap.

Applicazioni

Conducting polymer precursor.
It can be used as a monomer with 5,5′-dibromo-3,3′-dihexyl-2,2′-bithiophene, which can synthesize regioregular-P3HT-regiosymmetric-P3HT (a diblock polymer) for organic electronics based applications. It can also be used in the synthesis of P3HT, which can be potentially used for photocatalytic applications.

Note legali

Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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3-Hexylthiophene-2-boronic acid pinacol ester 95%

Sigma-Aldrich

697400

3-Hexylthiophene-2-boronic acid pinacol ester

3-Dodecylthiophene 97%

Sigma-Aldrich

456365

3-Dodecylthiophene

Charge Transport in Conjugated Polymers with Pendent Stable Radical Groups.
Zhang Y, et al.
Chemistry of Materials (2018)
Paulina Powroznik et al.
Sensors (Basel, Switzerland), 20(2) (2020-01-19)
In the present work, we report the use of regioregular poly(3-hexyltiophene) polymer (RR-P3HT) as a potential light-activated material for sensing the chemical nerve agent simulant dimethyl methylphosphonate (DMMP). The electrical response of thick films of RR-P3HT, deposited by spray-coating method
Tomasz Jarosz et al.
Polymers, 11(2) (2019-04-10)
A type of graft copolymer based on polysiloxane and regioregular poly(3-hexylthiophene) (P3HT) has been synthesised and its properties have been studied alongside those of its parent conjugated polymer-regioregular P3HT. Electrochemical analysis has revealed more significant changes in conformation of the
Xiaoyu Li et al.
Nature communications, 8, 15909-15909 (2017-06-27)
Micelles formed by the self-assembly of block copolymers in selective solvents have attracted widespread attention and have uses in a wide variety of fields, whereas applications based on their electronic properties are virtually unexplored. Herein we describe studies of solution-processable
Kinga Kepska et al.
Chemicke zvesti, 72(1), 251-259 (2018-01-26)
The first comprehensive spectroelectrochemical account of the behaviour of regioregular (RR-P3HT) and statistical (ST-P3HT) poly(3-hexylthiophenes) in solution is presented, in contrast to the many reports dealing with P3HT films merely deposited from solution. The conducted experiments revealed that the two
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