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171368-73-3

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171368-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 171368-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,3,6 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 171368-73:
(8*1)+(7*7)+(6*1)+(5*3)+(4*6)+(3*8)+(2*7)+(1*3)=143
143 % 10 = 3
So 171368-73-3 is a valid CAS Registry Number.

171368-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-1,4-didodecoxybenzene

1.2 Other means of identification

Product number -
Other names 1-bromo-2,5-didodecyloxybenzene

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:171368-73-3 SDS

171368-73-3Relevant articles and documents

Synthesis and Properties of Triphenodioxazine-Based Conjugated Polymers for Polymer Solar Cells

Gong, Xiaohui,Han, Pei,Wen, Hui,Sun, Ying,Zhang, Xueqin,Yang, Hong,Lin, Baoping

, p. 3689 - 3698 (2017/07/22)

As a fused-ring conjugated unit, triphenodioxazine, has been applied in two series of thiophene-free conjugated polymers for polymer solar cells. The polymers were synthesized through a multi-step synthetic route, and the substituents had a great effect on the reactivity of the reactants. Relationships among the polymer structures as well as thermal, optical, and electrochemical properties were investigated in detail by experimental data analysis and theoretical simulation. The polymers possess highly planar backbones, broad Vis/NIR absorption bands, suitable frontier molecular orbital energies, and low band gaps ranging from 1.3 to 1.8 eV. The power conversion efficiencies of their photovoltaic devices are about 1 %. Introducing longer alkyl side chains into a polymer can bring about a better film-forming ability and improve the photovoltaic performance.

Bi-directional synthesis of a series of 2,5-dodecanoxy-phenyleneethynylene oligomers

González-Rojano, Norma,Arias-Marín, Eduardo,Navarro-Rodríguez, Dámaso,Weidner, Steffen

, p. 1259 - 1262 (2007/10/03)

A family of rigid rod like 2,5-dodecanoxy-phenyleneethynylene oligomers having 3, 5, 7, and 9 repeating units was selectively synthesized by a bi-directional iterative divergent-convergent approach. Starting from a central 1,4-bis(dodecanoxy)-2,5-diiodobe

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