456373
2,5-Dibromo-3-hexylthiophene
97%
Sinônimo(s):
2,5-Dibromo-3-hex-1-ylthiophene
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5 G
R$ 812,00
25 G
R$ 2.812,00
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5 G
R$ 812,00
25 G
R$ 2.812,00
About This Item
Fórmula empírica (Notação de Hill):
C10H14Br2S
Número CAS:
Peso molecular:
326.09
Número MDL:
Código UNSPSC:
12352103
ID de substância PubChem:
NACRES:
NA.23
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Nível de qualidade
Ensaio
97%
índice de refração
n20/D 1.557 (lit.)
densidade
1.521 g/mL at 25 °C (lit.)
temperatura de armazenamento
2-8°C
cadeia de caracteres SMILES
CCCCCCc1cc(Br)sc1Br
InChI
1S/C10H14Br2S/c1-2-3-4-5-6-8-7-9(11)13-10(8)12/h7H,2-6H2,1H3
chave InChI
NSYFIAVPXHGRSH-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
Aplicação
Conducting polymer precursor.[3]
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.[4] It can also be used in the synthesis of P3HT, which can be potentially used for photocatalytic applications.[5]
Informações legais
Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.
Código de classe de armazenamento
10 - Combustible liquids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves
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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
Charge Transport in Conjugated Polymers with Pendent Stable Radical Groups.
Zhang Y, et al.
Chemistry of Materials (2018)
Evidence of Ni (0) complex diffusion during grignard metathesis polymerization of 2, 5-dibromo-3-hexylthiophene.
Achord BC and Rawlins JW
Macromolecules, 42(22), 8634-8639 (2009)
Uniform electroactive fibre-like micelle nanowires for organic electronics.
Li X, et al.
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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
Artigos
Oligothiophenes are important organic electronic materials which can be produced using synthetic intermediates and Suzuki coupling.
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