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Merck
모든 사진(1)

주요 문서

424285

Sigma-Aldrich

3-Octylthiophene

97%

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About This Item

실험식(Hill 표기법):
C12H20S
CAS Number:
Molecular Weight:
196.35
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

97%

양식

liquid

refractive index

n20/D 1.492 (lit.)

bp

106-107 °C/3 mmHg (lit.)

density

0.92 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCc1ccsc1

InChI

1S/C12H20S/c1-2-3-4-5-6-7-8-12-9-10-13-11-12/h9-11H,2-8H2,1H3

InChI key

WQYWXQCOYRZFAV-UHFFFAOYSA-N

일반 설명

3-Octylthiophene is an alkyl thiophene derivative. It has been synthesized by the reaction of 3-bromothiophene with octylmagnesium bromide.

애플리케이션

3-Octylthiophene may be used as a starting material in the synthesis of the following:
  • 2,5-dibromo-3-octylthiophene
  • poly(3-butylthiophene)-b-poly(3-octylthiophene), a diblock copoly(3-alkylthiophene)
  • regioregular poly(3-octylthiophene) (POT)

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

235.4 °F - closed cup

Flash Point (°C)

113 °C - closed cup

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


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시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

Slide 1 of 1

1 of 1

Crystalline diblock conjugated copolymers: Synthesis, self-assembly, and microphase separation of poly (3-butylthiophene)-b-poly (3-octylthiophene).
Wu PT, et al.
Macromolecules, 42(7), 2317-2320 (2009)
Soluble Phenanthrenyl-Imidazole-Presenting Regioregular Poly (3-octylthiophene) Copolymers Having Tunable Bandgaps for Solar Cell Applications.
Chang YT, et al.
Advances in Functional Materials, 17(16), 3326-3331 (2007)
New convenient synthesis of highly regioregular poly (3-octylthiophene) based on the Suzuki coupling reaction.
Guillerez S and Bidan G.
Synthetic Metals, 93(2), 123-126 (1998)
Nannan Jian et al.
Physical chemistry chemical physics : PCCP, 21(13), 7174-7182 (2019-03-20)
Conjugated fluorophores have been extensively used for fluorescence sensing of various substances in the field of life processes and environmental science, due to their noninvasiveness, sensitivity, simplicity and rapidity. Most existing conjugated fluorophores exhibit excellent light-emitting performance in dilute solutions

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