69104-74-1 Usage
Uses
Used in Pharmaceutical and Agrochemical Synthesis:
2-(benzo[d]thiazol-2-ylthio)aniline is used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique molecular structure allows for the development of new drugs and pesticides with improved efficacy and selectivity.
Used in Organic Synthesis:
2-(benzo[d]thiazol-2-ylthio)aniline serves as a versatile building block in organic synthesis, enabling the creation of a wide range of organic molecules with diverse applications.
Used in Dye and Pigment Development:
2-(benzo[d]thiazol-2-ylthio)aniline is used as a precursor in the development of dyes and pigments, offering novel color properties and improved performance characteristics.
Used in Materials Science:
2-(benzo[d]thiazol-2-ylthio)aniline has potential applications in materials science, where its unique properties can be harnessed to develop new materials with enhanced properties for various applications.
Research and Development:
Due to its unique molecular structure and properties, 2-(benzo[d]thiazol-2-ylthio)aniline is a subject of ongoing research to explore its potential uses and applications in various industries, including the development of new drugs, materials, and other chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 69104-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,1,0 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69104-74:
(7*6)+(6*9)+(5*1)+(4*0)+(3*4)+(2*7)+(1*4)=131
131 % 10 = 1
So 69104-74-1 is a valid CAS Registry Number.
69104-74-1Relevant academic research and scientific papers
Synthesis of heteroaryl containing sulfides via enaminone ligand assisted, copper-catalyzed C-S coupling reactions of heteroaryl thiols and aryl halides
Liu, Yunyun,Huang, Bin,Cao, Xiaoji,Wu, Dan,Wan, Jie-Ping
, p. 37733 - 37737 (2014/11/07)
The C-S cross coupling reactions between electron deficient heteroaryl thiols and aryl halides have been smoothly performed to provide various heteroaryl containing sulfides in the presence of copper catalyst and enaminone ligand. the Partner Organisations 2014.
Substrate-promoted ligand-free CuI catalyzed S-arylation of 2-mercaptobenzothiazoles with aryl iodides in water
He, Guozhen,Huang, Yuan,Tong, Yao,Zhang, Jie,Zhao, Dan,Zhou, Shuangli,Han, Shiqing
supporting information, p. 5318 - 5321 (2013/09/12)
A green and efficient method has been developed for the cross-coupling of 2-mercaptobenzothiazoles with aryl iodides in water. The reactions proceeded smoothly under ligand-free conditions in the presence of TBAB to give the corresponding products in good yields. The protocol showed good tolerance toward a variety of functional groups. A substrate-promoted mechanism for this catalytic reaction has been proposed.
