1843-22-7 Usage
General Description
Benzothiazol-2-yl-(2-methoxy-phenyl)-amine is a chemical compound with the molecular formula C15H13N3OS. It is a derivative of benzothiazole and contains a benzene ring with a methoxy group attached to it. BENZOTHIAZOL-2-YL-(2-METHOXY-PHENYL)-AMINE is commonly used in pharmaceutical and organic synthesis research for its potential therapeutic properties. It has been studied for its potential anti-cancer, anti-inflammatory, and anti-bacterial activities, making it an important target for drug development. Additionally, benzothiazol-2-yl-(2-methoxy-phenyl)-amine has also been investigated for its potential applications in the field of materials science, especially in the development of organic electronic devices and sensors.
Check Digit Verification of cas no
The CAS Registry Mumber 1843-22-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,4 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1843-22:
(6*1)+(5*8)+(4*4)+(3*3)+(2*2)+(1*2)=77
77 % 10 = 7
So 1843-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H12N2OS/c1-17-12-8-4-2-6-10(12)15-14-16-11-7-3-5-9-13(11)18-14/h2-9H,1H3,(H,15,16)
1843-22-7Relevant articles and documents
An "on-water" exploration of CuO nanoparticle catalysed synthesis of 2-aminobenzothiazoles
Rout, Saroj Kumar,Guin, Srimanta,Nath, Jayashree,Patel, Bhisma K.
, p. 2491 - 2498 (2013/02/21)
An "on-water" one-pot process has been engineered for the preparation of 2-aminobenzothiazole from ortho-halo (-F, -Cl, -Br and -I) substituted unsymmetrical thioureas. For ortho -I and -Br substrates the reactions afford 2-aminobenzothiazoles under metal free condition promoted by base. However, the relatively inert ortho -Cl and -F substrates undergo intramolecular arylthiolation only in the presence of CuO nanoparticles yielding 2-aminobenzothiazoles. This methodology provides easy access to aminobenzothiazoles utilising even the ortho -Cl and -F substrates. The catalyst is recyclable several times without loss of substantial activity. Other remarkable features include the wide range of functional group tolerance, absence of chromatographic purification (for ortho -I and -Br substrates) and providing moderate to excellent yield of the products under mild conditions, thus rendering the methodology as a highly eco-friendly alternative to the existing methods.