289470-44-6 Usage
Description
3-Thiophenecarboxylic acid, 2,5-dibromo-, ethyl ester (9CI), also known as Ethyl 2,5-dibromothiophene-3-carboxylate, is a derivative of thiophene carboxylic acid. 3-Thiophenecarboxylicacid,2,5-dibromo-,ethylester(9CI) features a thiophene ring with two bromine atoms at the 2nd and 5th positions and an ester group attached to the 3rd position. The carboxylate group acts as an electron-withdrawing group, which reduces the electron density at the thiophene ring. This property makes it a potentially useful compound in various chemical and pharmaceutical applications.
Uses
Used in Chemical Synthesis:
3-Thiophenecarboxylic acid, 2,5-dibromo-, ethyl ester (9CI) is used as an intermediate in the synthesis of various organic compounds. The electron-withdrawing nature of the carboxylate group and the presence of bromine atoms make it a versatile building block for creating a range of molecules with different properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Thiophenecarboxylic acid, 2,5-dibromo-, ethyl ester (9CI) is used as a starting material for the development of new drugs. The unique structure of this compound allows for the design of molecules with specific biological activities, such as potential therapeutic agents for various diseases.
Used in Material Science:
3-Thiophenecarboxylic acid, 2,5-dibromo-, ethyl ester (9CI) can be utilized in the development of novel materials with specific properties. The electron-withdrawing nature of the carboxylate group and the presence of bromine atoms can influence the electronic and optical properties of materials, making them suitable for applications in electronics, sensors, and other advanced technologies.
Used in Dye and Pigment Industry:
The unique structure of 3-Thiophenecarboxylic acid, 2,5-dibromo-, ethyl ester (9CI) can be exploited in the design of new dyes and pigments. The electron-withdrawing nature of the carboxylate group and the presence of bromine atoms can contribute to the color and stability of these compounds, making them suitable for use in various applications, such as inks, paints, and textiles.
Check Digit Verification of cas no
The CAS Registry Mumber 289470-44-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,4,7 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 289470-44:
(8*2)+(7*8)+(6*9)+(5*4)+(4*7)+(3*0)+(2*4)+(1*4)=186
186 % 10 = 6
So 289470-44-6 is a valid CAS Registry Number.