399051
3-Hexylthiophene
≥99%
동의어(들):
3-Hexylthiophene
로그인조직 및 계약 가격 보기
크기 선택
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C10H16S
CAS 번호:
Molecular Weight:
168.30
Beilstein:
1617129
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
분석
≥99%
양식
liquid
refractive index
n20/D 1.496 (lit.)
bp
65 °C/0.45 mmHg (lit.)
density
0.936 g/mL at 25 °C (lit.)
SMILES string
CCCCCCc1ccsc1
InChI
1S/C10H16S/c1-2-3-4-5-6-10-7-8-11-9-10/h7-9H,2-6H2,1H3
InChI key
JEDHEMYZURJGRQ-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
3-Hexylthiophene, a sulfur containing heterocyclic building block, is a thiophene derivative. Poly(3-hexylthiophene) (P3HT) nanofibres have been used for the preparation of organic phototransistors (OPTs).
애플리케이션
3-Hexylthiophene may be used as starting reagent in the synthesis of poly(3-hexylthiophene) (P3HT).
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
X-ray and electron induced oligomerization of condensed 3-hexylthiophene.
Hernandez JE, et al.
The Journal of Physical Chemistry B, 105(35), 8339-8344 (2001)
A photochemical study of poly (3-hexylthiophene).
Holdcroft S.
Macromolecules, 24(17), 4839-4844 (1991)
Karolina Gebka et al.
Polymers, 11(2) (2019-04-10)
Electrochemical polymerisation is reported to be a method for readily producing copolymers of various conjugated molecules. We employed this method for mixtures of indole, carbazole or fluorene with 3-hexylthiophene (HT), in order to obtain their soluble copolymers. Although polymer films
Fangwen Zha et al.
Soft matter, 16(28), 6591-6598 (2020-07-01)
The fabrication of scaffolds with suitable chemical, physical, and electrical properties is critical for nerve cell adhesion and proliferation. Recently, electrical stimulation on conductive polymers has been applied to construct functional nerve cell scaffolds. Herein, we prepared natural polymer (cellulose)/conductive
Thien An Phung Hai et al.
Carbohydrate polymers, 179, 221-227 (2017-11-08)
Surface functionalization of cellulose with poly(3-hexylthiophene) (P3HT) was conducted with FeCl
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