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144012-09-9 Usage

Chemical Properties

Light yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 144012-09-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,0,1 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 144012-09:
79 % 10 = 9
So 144012-09-9 is a valid CAS Registry Number.



According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017


1.1 GHS Product identifier

Product name 2-Bromo-3-decylthiophene

1.2 Other means of identification

Product number -
Other names 2-Bromo-3-decylthiophen

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:144012-09-9 SDS

144012-09-9Relevant articles and documents

A crystalline D-π-A organic small molecule with naphtho[1,2-b:5,6- b′]dithiophene-core for solution processed organic solar cells

Dutta, Pranabesh,Park, Hanok,Lee, Woo-Hyoung,Kang, In-Nam,Lee, Soo-Hyoung

, p. 3183 - 3194 (2012)

In this work, we have designed and synthesized a new naphtho[1,2-b:5,6- b′]dithiophene-containing enlarged π-conjugated donor-acceptor (D-A) small molecule, NDT(TTz)2, for use in solution-processed organic photovoltaics. NDT(TTz)2, which contains a thiophene-bridged naphtho[1,2-b:5,6-b′]dithiophene as the central fused core and triphenylamine-flanked thiophene thiazolothiazole as a spacer, was synthesized via sequential Suzuki and Stille coupling reactions. The thermal, physiochemical, and electrochemical properties of NDT(TTz)2 have been evaluated by differential scanning calorimetry, thermogravimetry, UV-Vis spectroscopy, photoluminescence spectroscopy, X-ray diffraction, and cyclic voltammetry. As desired for photovoltaic applications, NDT(TTz)2 possesses good solubility, thermal stability, and a well-ordered, π-π stacked, crystallinity. The optical band gap and HOMO level of NDT(TTz) 2 were determined to be 2.0 eV and -5.23 eV, respectively. In addition to organic thin film transistor studies, application of NDT(TTz) 2 to preliminary photovoltaic devices has also been investigated by fabricating solution-processed bulk heterojunction solar cells together with PC71BM in a typical layered device structure, ITO/PEDOT:PSS/NDT(TTz) 2:PC71BM/LiF/Al. Without extensive optimization of the device, NDT(TTz)2 in these devices shows a maximum power conversion efficiency of 1.44% under AM 1.5 illumination at a 100 mW/cm2 intensity.

Novel s-tetrazine-based dyes with enhanced two-photon absorption cross-section

Quinton, Cassandre,Chi, San-Hui,Dumas-Verdes, Ccile,Audebert, Pierre,Clavier, Gilles,Perry, Joseph W.,Alain-Rizzo, Valrie

, p. 8351 - 8357 (2015/08/18)

This paper reports the synthesis and the linear and non-linear absorption properties of a series of new tetrazine-based D-π-A-π-D and D-π-A type dyes. In these derivatives, a central tetrazine core was connected with one or two terminal triphenylamine moi

A bolaamphiphilic sexithiophene with liquid crystalline triangular honeycomb phase

Bu, Wei,Gao, Hongfei,Tan, Xiaoping,Dong, Xing,Cheng, Xiaohong,Prehm, Marko,Tschierske, Carsten

, p. 1756 - 1758 (2013/03/14)

A new bolaamphiphile comprising a 5,5′′′′′- diphenyl-sexithiophene core with glycerol groups at each end and four lateral decyl chains was synthesized, which self-assembles into a liquid crystalline phase representing a nanoscale honeycomb composed of qua

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