33761-31-8 Usage
Uses
Used in Pharmaceutical Synthesis:
2-Amino-6-methylpyridine-3-thiol is utilized as a building block in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents. Its unique structure allows for the creation of diverse chemical entities with potential medicinal properties.
Used in Agrochemical Production:
In the agrochemical industry, 2-Amino-6-methylpyridine-3-thiol serves as a key component in the synthesis of various agrochemicals. Its incorporation aids in the development of effective pesticides, herbicides, and other agricultural chemicals that enhance crop protection and yield.
Used in Dye Manufacturing:
2-Amino-6-methylpyridine-3-thiol is employed as a building block in the production of dyes, where its chemical structure contributes to the creation of vibrant and stable colorants used in various industries, including textiles, plastics, and printing.
Used in Materials Science:
Within the field of materials science, 2-Amino-6-methylpyridine-3-thiol has potential applications in the development of new materials with unique properties. Its versatility allows for the engineering of materials with tailored characteristics for specific applications.
Used in Organic Synthesis:
As a versatile reagent, 2-Amino-6-methylpyridine-3-thiol is used in organic synthesis to facilitate the formation of complex organic molecules. Its presence in reactions can enhance the synthesis process, leading to the production of a wide range of organic compounds for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 33761-31-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,7,6 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33761-31:
(7*3)+(6*3)+(5*7)+(4*6)+(3*1)+(2*3)+(1*1)=108
108 % 10 = 8
So 33761-31-8 is a valid CAS Registry Number.
33761-31-8Relevant academic research and scientific papers
Synthesis of analogues of the 2,3,6-triazaphenothiazine ring system
Okafor,Castle
, p. 199 - 203 (2007/10/02)
Treatment of 2,3-dichloroquinoxalines with 2-amino-6-picoline-3-thiol gave a mixture of 2,3-bis(2-amino-6-picolinyl-3-thio)quinoxalines (16, R = H, Cl) and 2,3-bis (N,N-dimethylamino)quinoxalines (15, R = H, Cl) separated by fractional crystallization. A similar reaction of 3-amino-6-methoxypyridine-2(1H)-thione (9) with 4,5-dichloropyridazin-3(2H)-one (21) gave 4-chloro-5-(3-amino-6-methoxypyridyl-2-thio)pyridazin-3(2H)-one (22). Concentrated hydrochloric acid-catalysed cyclization of 22 gave the nonrearranged 7-methoxy-2,3,6-triazaphenothiazin-1(2H)-one. The action of compound 22 in refluxing glacial acetic acid gave, on the other hand, 7-methoxy-2,3,6-triazaphenothiazin-4(3H)-one via a Smiles rearrangement. These cyclized compounds are the first known derivatives of the new 2,3,6-triazaphenothiazine ring system.
4,4'-Stilbenebis-pyridooxazoles and related optical brighteners and polymeric compositions brightened thereby
-
, (2008/06/13)
4,4'-Stilbenebis-2-oxazolopyridines, -2-thiazolopyridines, and 2-imidazopyridines are optical brightening agents useful for whitening and brightening natural and synthetic fibers, papers, resins and the like. The compounds are conveniently prepared by int
