143667-61-2 Usage
Uses
Used in Scientific Research:
2-Aminothiazolo[4,5-c]quinoline is used as a research chemical for [application reason], such as studying its chemical properties, reactivity, and potential interactions with other compounds. Its complex structure makes it a valuable subject for investigation in the field of organic chemistry.
Used in Chemical Synthesis:
2-Aminothiazolo[4,5-c]quinoline is used as a building block or intermediate in the synthesis of more complex molecules for [application reason], such as the development of new pharmaceuticals, agrochemicals, or materials with specific properties.
Used in Material Science:
2-Aminothiazolo[4,5-c]quinoline is used as a component in the development of new materials with unique properties for [application reason], such as creating novel polymers, dyes, or sensors that can be used in various industries.
Used in Pharmaceutical Development:
2-Aminothiazolo[4,5-c]quinoline is used as a potential drug candidate or a key intermediate in the synthesis of pharmaceutical compounds for [application reason], such as treating diseases or improving the efficacy of existing medications.
Used in Agrochemical Industry:
2-Aminothiazolo[4,5-c]quinoline is used as a component in the development of new agrochemicals for [application reason], such as creating more effective pesticides, herbicides, or plant growth regulators.
Note: The specific application reasons for each use should be filled in based on the actual research findings or intended applications of 2-Aminothiazolo[4,5-c]quinoline.
Check Digit Verification of cas no
The CAS Registry Mumber 143667-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,6,6 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 143667-61:
(8*1)+(7*4)+(6*3)+(5*6)+(4*6)+(3*7)+(2*6)+(1*1)=142
142 % 10 = 2
So 143667-61-2 is a valid CAS Registry Number.
143667-61-2Relevant articles and documents
Convenient synthesis of 2-aminonaphthalene-1-thiol and 3-aminoquinoline-4-thiol and cyclocondensations to 1,4-thiazino and 1,4-thiazepino derivatives
Ambrogi,Grandolini,Perioli,Rossi
, p. 656 - 658 (2007/10/02)
An improved method for the synthesis of 2-aminonaphthalene-1-thiol and an alternative procedure for the preparation of 3-aminoquinoline-4-thiol are described. From these intermediates some 1,4-thiazino and 1,4-thiazepino tricyclic derivatives have been prepared.
