153137-85-0 Usage
Uses
Used in Pharmaceutical Industry:
3-Amino-5-methylthiophene serves as a crucial intermediate in the synthesis of various pharmaceuticals, leveraging its reactive amino and methylthio groups to form complex molecular structures that address specific medical needs.
Used in Agrochemical Industry:
In agrochemicals, 3-Amino-5-methylthiophene is utilized as an intermediate to develop compounds that can protect crops from pests and diseases, capitalizing on its ability to be incorporated into a variety of chemical frameworks.
Used in Dye Industry:
3-Amino-5-methylthiophene is employed in the production of dyes, where its structural features contribute to the color and properties of the final dye products, offering a broad spectrum of applications in textiles, inks, and other industries.
Used in Materials Science:
3-Amino-5-methylthiophene is used as a building block in the development of organic semiconductors and conducting polymers, thanks to its potential to influence the electronic properties of these materials, which is vital for applications in electronic devices and sensors.
These applications highlight the diverse utility of 3-Amino-5-methylthiophene across different sectors, underscoring its importance in the synthesis and development of new materials and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 153137-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,1,3 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 153137-85:
(8*1)+(7*5)+(6*3)+(5*1)+(4*3)+(3*7)+(2*8)+(1*5)=120
120 % 10 = 0
So 153137-85-0 is a valid CAS Registry Number.
153137-85-0Relevant academic research and scientific papers
Synthesis of 2-carbamoylthieno[3,2-d]thiazoles
Yarovenko,Smirnova,Bulgakova,Zavarzin,Krayushkin
, p. 1161 - 1163 (2007/10/03)
A preparation procedure was developed for previously unknown 2-carbamoylthieno[3,2-d]-thiazoles consisting in cyclization effected by K 3Fe(CN)6 of monothiooxamides obtained from 2-methyl-4-aminothiophene, chloroacetamides, and sulfur in the presence of triethylamine.
