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3-Thiophenecarboxylic acid, 4-formyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53686-05-8

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53686-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53686-05-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,8 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53686-05:
(7*5)+(6*3)+(5*6)+(4*8)+(3*6)+(2*0)+(1*5)=138
138 % 10 = 8
So 53686-05-8 is a valid CAS Registry Number.

53686-05-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-formylthiophene-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Thiophenecarboxylic acid,4-formyl

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:53686-05-8 SDS

53686-05-8Relevant academic research and scientific papers

Effect of oxygen-containing functional side chains on the electronic properties and photovoltaic performances in a thiophene-thiazolothiazole copolymer system

Saito, Masahiko,Osaka, Itaru,Koganezawa, Tomoyuki,Takimiya, Kazuo

, p. 556 - 564 (2014)

We report the synthesis and characterization of new thiazolothiazole-based semiconducting polymers with alkoxy and/or ester groups as the side chain. An introduction of the alkoxy groups raised the HOMO energy level of the polymers, whereas the introduction of the ester groups lowered the LUMO energy level. It is found that, interestingly, in the monomers the electronic effect of the ester group was more significant than that of the alkoxy groups, whereas in the polymers the effect of the alkoxy group was more significant. PTzBT-oBOeHD with both the alkoxy and ester groups gave the most redshifted absorption spectrum compared to the polymers with the alkyl and alkoxy groups (PTzBT-oBOHD) and with the alkyl and ester groups (PTzBT-BOeHD). Solar cells using PTzBT-oBOeHD gave the highest power conversion efficiencies of up to 4.5% with the highest short-circuit current density (JSC) of 10.9 mA/cm2 among those with the newly synthesized polymers.

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