122333-32-8 Usage
Description
1H-1,2,4-Triazol-5-ol(9CI) is a chemical compound characterized by the molecular formula C2H3N3O. It is a member of the triazole class, featuring a five-membered ring structure composed of nitrogen and oxygen atoms. 1H-1,2,4-Triazol-5-ol(9CI) is recognized for its versatility and significance as an intermediate in the synthesis of a wide range of chemical compounds, including pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
1H-1,2,4-Triazol-5-ol(9CI) is utilized as a precursor in the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 1H-1,2,4-Triazol-5-ol(9CI) serves as a starting material for the production of different agrochemicals. Its role in this industry is crucial for the creation of effective solutions for agricultural applications.
Used in Organic Chemistry:
1H-1,2,4-Triazol-5-ol(9CI) is also employed as a building block in organic chemistry. It enables the construction of more complex molecules, which can be used in various chemical processes and products, highlighting its importance in the field of organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 122333-32-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,3 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 122333-32:
(8*1)+(7*2)+(6*2)+(5*3)+(4*3)+(3*3)+(2*3)+(1*2)=78
78 % 10 = 8
So 122333-32-8 is a valid CAS Registry Number.
122333-32-8Relevant articles and documents
Gas-phase elimination reactions of 4-arylideneimino-1,2,4-triazol-3(2H)-ones and their 3(2H)-thione analogues
Al-Awadi, Nouria,Ibrahim, Yehia,Kaul, Kamini,Dib, Hicham
, p. 521 - 525 (2007/10/03)
4-Arylideneimino-1,2,4-triazol-3(2H)-ones (1-4) and their thio analogues (5-8) were pyrolysed in the gas phase. The reactions were homogeneous and free from catalytic and radical pathways. Analysis of the pyrolysate showed the elimination products to be substituted benzonitriles and the corresponding 3-hydroxy-1,2,4-triazoles and their thio analogues. The kinetic results and product analysis lend support to a reaction pathway involving a six-membered transition state. At 500 K, the thiooxotriazoles 5-8 were found to be 103-fold more reactive than the corresponding oxotriazoles 1-4. The reactivities of the 2-oxotriazoles were compared with those of the substituted 2-oxopyridine-3-carbonitriles.
