30358-18-0 Usage
Description
2-AMINO-4-METHOXY-6-(METHYLTHIO)-1,3,5-TRIAZINE is a triazine derivative chemical compound with the molecular formula C5H8N4OS. It features an amino group, a methoxy group, and a methylthio group, making it a versatile building block for various applications across different industries.
Uses
Used in Pharmaceutical Industry:
2-AMINO-4-METHOXY-6-(METHYLTHIO)-1,3,5-TRIAZINE is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into drug molecules, potentially enhancing their therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2-AMINO-4-METHOXY-6-(METHYLTHIO)-1,3,5-TRIAZINE is utilized as a precursor in the development of agrochemicals, contributing to the creation of effective products for agricultural applications.
Used in Dye Industry:
2-AMINO-4-METHOXY-6-(METHYLTHIO)-1,3,5-TRIAZINE is employed as a key component in the production of dyes, where its unique structure allows for the creation of diverse colorants for various uses.
Used in Materials Science:
2-AMINO-4-METHOXY-6-(METHYLTHIO)-1,3,5-TRIAZINE has potential applications in materials science, where it can be used to develop new materials with specific properties, such as improved stability or reactivity.
Used in Organic Synthesis:
As a building block for organic synthesis, 2-AMINO-4-METHOXY-6-(METHYLTHIO)-1,3,5-TRIAZINE is a valuable component in the creation of complex organic molecules for a wide range of applications.
Check Digit Verification of cas no
The CAS Registry Mumber 30358-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,5 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30358-18:
(7*3)+(6*0)+(5*3)+(4*5)+(3*8)+(2*1)+(1*8)=90
90 % 10 = 0
So 30358-18-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N4OS/c1-10-4-7-3(6)8-5(9-4)11-2/h1-2H3,(H2,6,7,8,9)
30358-18-0Relevant articles and documents
Synthesis and Structure Elucidation of 3-Methoxy-1-methyl-1H-1,2,4-triazol-5-amine and 5-Methoxy-1-methyl-1H-1,2,4-triazol-3-amine
Selby, T. P.,Lepone, G. E.
, p. 61 - 64 (2007/10/02)
Previously it was shown that condensation of dimethyl N-cyanodithioimidocarbonate (1a) with methylhydrazine gave predominantly 1-methyl-5-methylthio-1H-1,2,4-triazol-3-amine (2), which was initially identified erroneously as the regioisomer 1-methyl-3-methylthio-1H-1,2,4-triazol-5-amine (3).We have found that reaction of dimethyl N-cyanoimidocarbonate (1b) with methyl hydrazine affords a high yield of 3-methoxy-1-methyl-1H-1,2,4-triazol-5-amine (4) rather than the regioisomer 5-methoxy-1-methyl-1H-1,2,4-triazol-3-amine (5).The structure assignement of 4 was confirmedby X-ray crystallographic analysis of the benzenesulfonyl isocyanate adduct 7.Triazole 5 was obtained after reacting dimethyl N-cyanothioimidocarbonate (1c) with methylhydrazine.
