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479243-27-1

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479243-27-1 Usage

Description

5-(2-Methoxy-phenyl)-thiophene-2-carbaldehyde is a chemical compound characterized by a molecular formula of C12H10O2S. It is a thiophene derivative featuring a substituted aldehyde group and a methoxy-phenyl group, which endows it with unique electronic and optical properties. 5-(2-METHOXY-PHENYL)-THIOPHENE-2-CARBALDEHYDE is recognized for its potential in various scientific and industrial applications due to its structural and functional attributes.

Uses

Used in Pharmaceutical and Agrochemical Industries:
5-(2-Methoxy-phenyl)-thiophene-2-carbaldehyde is utilized as a building block in the synthesis of a variety of organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure allows it to be a key component in the creation of new molecules with therapeutic or pesticidal properties.
Used in Materials Science:
In the field of materials science, 5-(2-Methoxy-phenyl)-thiophene-2-carbaldehyde is employed for its potential to contribute to the development of advanced materials. Its electronic and optical characteristics make it a candidate for use in the design of materials with specific properties tailored for various applications.
Used in Organic Electronics:
5-(2-METHOXY-PHENYL)-THIOPHENE-2-CARBALDEHYDE also finds use in organic electronics, where its unique properties can be leveraged to improve the performance of electronic devices. Its potential applications in this field include the development of organic semiconductors, which are crucial for flexible electronics and other emerging technologies.
Used as a Fluorescent Label or Dye in Biological and Medical Research:
5-(2-Methoxy-phenyl)-thiophene-2-carbaldehyde may also serve as a fluorescent label or dye in biological and medical research. Its optical properties could be harnessed for imaging and tracking purposes, contributing to advancements in diagnostic and therapeutic methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 479243-27-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,9,2,4 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 479243-27:
(8*4)+(7*7)+(6*9)+(5*2)+(4*4)+(3*3)+(2*2)+(1*7)=181
181 % 10 = 1
So 479243-27-1 is a valid CAS Registry Number.

479243-27-1SDS

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 5-(2-methoxyphenyl)thiophene-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 5-(2-methoxyphenyl)-2-thiophenecarbaldehyde

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:479243-27-1 SDS

479243-27-1Downstream Products

479243-27-1Relevant articles and documents

Copper-catalyzed direct C-H arylation of thieno[3,4-c]pyrrole-4,6-dione (TPD): Toward efficient and low-cost synthesis of ??-functional small molecules

Song, Yi-Ting,Lin, Po-Han,Liu, Ching-Yuan

supporting information, p. 3761 - 3768 (2015/02/19)

A series of thieno[3,4-c]pyrrole-4,6-dione (TPD)-based functional small molecules were efficiently synthesized through direct C-H arylations using inexpensive copper salts. In this study, we examined all required reaction parameters including various copper complexes, ligands, bases, and (co)-solvents. Under the optimum reaction conditions, the C-H arylation proceeded smoothly and a variety of functional groups such as ester, nitrile, fluoride, chloride, triazene, and amine were tolerated. This method provides a step-economical and relatively low-cost synthetic alternative to presently used coupling reactions for the preparation of TPD-containing p-functional materials.

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