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Merck
모든 사진(2)

주요 문서

750042

Sigma-Aldrich

1,3,5-Tris(2-thienyl)benzene

97%

동의어(들):

1,3,5-Tri(thiophen-2-yl)benzene

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About This Item

실험식(Hill 표기법):
C18H12S3
CAS Number:
Molecular Weight:
324.48
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.23

분석

97%

양식

solid

mp

154-160 °C

SMILES string

c1csc(c1)-c2cc(cc(c2)-c3cccs3)-c4cccs4

InChI

1S/C18H12S3/c1-4-16(19-7-1)13-10-14(17-5-2-8-20-17)12-15(11-13)18-6-3-9-21-18/h1-12H

InChI key

UBHPRZXDFVCNHZ-UHFFFAOYSA-N

일반 설명

1,3,5-Tris(2-thienyl)benzene is a 1,3,5 tris substituted benzene that has a three dimensional structure which facilitates the preparation of conjugating polymers. It is a branched conductive monomer with electronically attached nodes that provide a suitable support to increase the conductivity of the synthesized polymers.[1][2]

애플리케이션

1,3,5-Tris(2-thienyl)benzene is a trifunctionalized monomer that can be used in the synthesis of conjugated C3-symmetric poly(arylbenzene) polymers. These polymeric materials can further be used in organic photovoltaic devices as well as organic field effect transistors (OFETs) and organic light emitting diodes (OLED) systems.[3][4]

픽토그램

Skull and crossbones

신호어

Danger

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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시험 성적서(COA)

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

Shape and size effects in the crystal structures of complexes of 1, 3, 5-trinitrobenzene with some trigonal donors: the benzene-thiophene exchange rule
Thallapally PK, et al.
Tetrahedron, 56(36), 6721-6728 (2000)
Electrochemical and spectral properties of meta-linked 1, 3, 5-tris (aryl) benzenes and 2, 4, 6-tris (aryl)-1-phenoles, and their polymers
Idzik KR, et al.
Electrochimica Acta, 55(24), 7419-7426 (2010)
Synthesis of C3-Symmetric Nano-Sized Polyaromatic Compounds by Trimerization and Suzuki- Miyaura Cross-Coupling Reactions
Kotha S, et al.
European Journal of Organic Chemistry, 2004(19), 4003-4013 (2004)
Idzik, K. R.; Beckert, R.; Golba, S.; Ledwon, P.; Lapkowski, M.
Tetrahedron Letters, 51, 2396-2396 (2010)
Synthesis and Electrochemical Properties of Novel 1, 3, 5-Tris (oligothienyl) benzenes: A New Generation of 3D Reticulating Agents
Cherioux F and Guyard L
Advances in Functional Materials, 11(4), 305-309 (2001)

문서

Organic materials in optoelectronic devices like LEDs and solar cells are of significant academic and commercial interest.

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