27282-89-9 Usage
Uses
Used in Organic Synthesis:
4-(Methylthio)-1,3,5-triazin-2-amine is utilized as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure and functional groups contribute to the formation of new materials with distinct properties.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 4-(methylthio)-1,3,5-triazin-2-amine is used as a precursor in the synthesis of drugs. Its chemical versatility allows for the development of compounds with specific therapeutic effects, addressing a range of medical needs.
Used in Agrochemical Development:
4-(Methylthio)-1,3,5-triazin-2-amine is employed in the agrochemical sector for the production of pesticides and other crop protection agents. Its role in these applications is to provide effective control over pests and diseases, ensuring crop health and productivity.
Used in Dye Manufacturing:
4-(methylthio)-1,3,5-triazin-2-amine is also used in the dye industry, where it serves as a starting material for the synthesis of various dyes. The dyes produced using 4-(methylthio)-1,3,5-triazin-2-amine are utilized in a wide range of applications, including textiles, plastics, and printing inks.
Used in Material Development:
The presence of the amine group in 4-(methylthio)-1,3,5-triazin-2-amine allows for further derivatization, making it a valuable component in the development of new materials with tailored properties for specific applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 27282-89-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,8 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27282-89:
(7*2)+(6*7)+(5*2)+(4*8)+(3*2)+(2*8)+(1*9)=129
129 % 10 = 9
So 27282-89-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H6N4S/c1-9-4-7-2-6-3(5)8-4/h2H,1H3,(H2,5,6,7,8)
27282-89-9Relevant academic research and scientific papers
NOVEL COMPOUNDS
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Page 37-38, (2010/02/08)
The invention relates to pyridine derivatives of formula (I) where the variables are defined in the specification.Processes for the preparation of these compounds together with pharmaceutical compositions containing them and their use in therapy in particular in the modulation of autoimmune disease is also described.
NOVEL COMPOUNDS
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Page 26-27, (2010/02/08)
The invention relates to pyridine derivatives, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.
Synthese regiospecifique d'acyl-4 pyrazoles a partir d'acyl-5 pyrimidines
Bajnati, Abdelilah,Kokel, Bruno,Hubert-Habart, Michel
, p. 318 - 324 (2007/10/02)
The transformation of variously substituted 5-acetyl-4-methylpyrimidines 1 into 4-acetyl-1-amidino-3-methylpyrazole amidinohydrazone dihydrochloride 3, under the action of amidinohydrazine hydrochloride, in boiling acidic methanolic solution, depends on the nature of the 2-substituent of pyrimidines 1, and on the stability of the amidinohydrazone of pyrimidines 2 under the reaction conditions.Phenylhydrazine transforms all the pyrimidines 1 into pyrazoles, regiospecifically or not, according to the nature of the 2-substituent of pyrimidines 1.This new possibility of ring contraction has been extended to other unsymetrical 5-acyl- and 5-ethoxycarbonylpyrimidines.
