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butyl 3-thienylacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94023-52-6

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94023-52-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94023-52-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,2 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 94023-52:
(7*9)+(6*4)+(5*0)+(4*2)+(3*3)+(2*5)+(1*2)=116
116 % 10 = 6
So 94023-52-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O2S/c1-2-3-5-12-10(11)7-9-4-6-13-8-9/h4,6,8H,2-3,5,7H2,1H3

94023-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name butyl 2-thiophen-3-ylacetate

1.2 Other means of identification

Product number -
Other names EINECS 301-650-0

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:94023-52-6 SDS

94023-52-6Downstream Products

94023-52-6Relevant academic research and scientific papers

Synthesis and photovoltaic properties of copolymers based on benzo[1,2-b:4,5-b′]dithiophene and thiophene with electron-withdrawing side chains

Nie, Yujuan,Zhao, Bin,Tang, Peng,Jiang, Peng,Tian, Zongfang,Shen, Ping,Tan, Songting

experimental part, p. 3604 - 3614 (2012/05/05)

Six alternating conjugated copolymers (PL1-PL6) of benzo[1,2-b:4,5- b′]dithiophene (BDT) and thiophene, containing electron-withdrawing oxadiazole (OXD), ester, or alkyl as side chains, were synthesized by Stille coupling reaction. The structures of the polymers were confirmed, and their thermal, optical, electrochemical, and photovoltaic properties were investigated. The introduction of conjugated electron-withdrawing OXD or formate ester side chain benefits to decrease the bandgaps of the polymers and improve the photovoltaic performance due to the low steric hindrance of BDT. Bulk heterojunction polymer solar cells (PSCs) were fabricated based on the blend of the as-synthesized polymers and the fullerene derivative [6,6]-phenyl-C 61-butyric acid methyl ester (PC61BM) in a 1:2 weight ratio. The maximum power conversion efficiency of 2.06% was obtained for PL5-based PSC under the illumination of AM 1.5, 100 mW/cm2.

Synthesis of functionalized thiophenes for the preparation of conducting polymer films with complexing properties

Brembilla,Collard,Henry,Jadamiec,Lapkowski,Matlengiewicz,Rodehueser

, p. 723 - 734 (2007/10/03)

Four series of novel substituted thiophenes (Schiff bases, esters, amides, and amino acids) have been synthesized and tested for their ability to form conducting polymer films via cyclic voltammetry in order to obtain electrochemical sensors for metal cations. The influence of the nature and size of the substituents on the electropolymerizability of the monomers has been studied. Copyright Taylor & Francis Group, LLC.

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