51291-82-8 Usage
Description
5-METHOXY-2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONE is an organic compound that serves as a crucial intermediate in the synthesis of various chemical compounds, particularly in the pharmaceutical and agricultural industries. Its molecular structure allows it to be a versatile building block for the development of new molecules with potential applications in different fields.
Uses
Used in Pharmaceutical Industry:
5-METHOXY-2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONE is used as an intermediate in the synthesis of 4-Desmethyl Flucarbazone Sodium Salt (D343230), which is an impurity of Flucarbazone (F148340) and Flucarbazone-sodium (F421125). These compounds have potential applications in the development of new pharmaceuticals, contributing to the advancement of drug discovery and therapeutic treatments.
Used in Agricultural Industry:
5-METHOXY-2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONE is used as a key component in the synthesis of Flucarbazone, which is a herbicide used for agricultural purposes. Flucarbazone helps in controlling and managing unwanted plant growth, ensuring better crop yield and quality. Its use in agriculture contributes to more efficient and sustainable farming practices.
Additionally, Flucarbazone is also recognized as an antiparasitic agent, which means that 5-METHOXY-2,4-DIHYDRO-3H-1,2,4-TRIAZOL-3-ONE, through its role in the synthesis of Flucarbazone, indirectly contributes to the development of antiparasitic treatments. This highlights the compound's potential in addressing various health and environmental concerns through its applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 51291-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,2,9 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51291-82:
(7*5)+(6*1)+(5*2)+(4*9)+(3*1)+(2*8)+(1*2)=108
108 % 10 = 8
So 51291-82-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H5N3O2/c1-8-3-4-2(7)5-6-3/h1H3,(H2,4,5,6,7)
51291-82-8Relevant articles and documents
Chlorination and subsequent cyclization to 1,3,4-oxadiazoles of N1-acyl-N3-cyanoguanidines and rerated compounds
Suyama, Takayuki,Hasegawa, Tadashi,Oda, Motokazu,Tomaru, Masahiko,Ohkoshi, Hiroyuki
, p. 121 - 129 (2007/10/03)
N1-Acyl-, N1-alkoxycarbonyl-, and N1-(N,N-dialkylcarbamoyl)guanidines bearing electron-withdrawing cyano or sulfonyl group at the N3-position were found to provide corresponding rearranged products, 1,3,4-oxadiazoles, when these guanidines were chlorinated by sodium hypochlorite followed by treating with base. Assignments of obtained compounds were accomplished by means of some reactions such as acid hydrolysis, alkoholysis, and catalytic hydrogenations, and of MS spectra.
Process for preparing alkoxytriazolinones
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, (2008/06/13)
Alkoxytriazolinones of the formula (I) ?known for example as intermediates for preparing agrochemically active compounds! STR1 wherein R represents an alkyl group, an alkenyl group, an alkinyl group, a cycloalkyl group, a cycloalkylalkyl group, an aryl group or an arylalkyl group, any of which may be substituted, are prepared by reacting a) thioimidodicarboxylic diesters of the general formula (II) STR2 wherein R is as defined above and R1 represents an alkyl group, an arylalkyl group or an aryl group, any of which may be substituted, with b) hydrazine, hydrazine hydrate or an acid adduct of hydrazine. The reaction is conducted i) in the presence of a diluent and, optionally, in the presence of a basic reaction auxiliary, and ii) at temperatures between -10° C. and +100° C.
