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Merck
모든 사진(1)

주요 문서

456373

Sigma-Aldrich

2,5-Dibromo-3-hexylthiophene

97%

동의어(들):

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

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크기 선택

5 G
₩312,417
25 G
₩1,104,625

₩312,417


출고 가능일2025년 4월 11일세부사항


벌크 견적 요청

크기 선택

보기 변경
5 G
₩312,417
25 G
₩1,104,625

About This Item

실험식(Hill 표기법):
C10H14Br2S
CAS Number:
Molecular Weight:
326.09
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.23

₩312,417


출고 가능일2025년 4월 11일세부사항


벌크 견적 요청

분석

97%

refractive index

n20/D 1.557 (lit.)

density

1.521 g/mL at 25 °C (lit.)

저장 온도

2-8°C

SMILES string

CCCCCCc1cc(Br)sc1Br

InChI

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

InChI key

NSYFIAVPXHGRSH-UHFFFAOYSA-N

일반 설명

2,5-Dibromo-3-hexylthiophene is a 2,5 coupled conductive polymer with conjugated polythiophene based system, which has a controllable band gap.[1][2]

애플리케이션

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]

법적 정보

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

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves


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문서 라이브러리 방문

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.
Nature Communications, 8(22), 15909-15909 (2017)
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

문서

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

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