123313-07-5 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 5 carbon (C), 7 hydrogen (H), 5 nitrogen (N), and 1 oxygen (O) atoms.
Explanation
This compound is a derivative of the heterocyclic compound triazine, which contains a six-membered ring with three nitrogen atoms and three carbon atoms. The compound has a methyl group (-CH3) at the 6th position and an amino group (-NH2) at the 4th position.
Explanation
The compound contains a triazine ring, which is a heterocyclic ring with alternating nitrogen and carbon atoms. It also has an amino group attached to the 4th position of the triazine ring and a methyl group at the 6th position.
Explanation
The compound is commonly used as a building block in the synthesis of various biologically active compounds, including those used in the pharmaceutical and agrochemical industries. It also has potential applications in the field of organic chemistry and has been studied for its pharmacological and biological activities.
Explanation
The compound has been studied for its potential pharmacological and biological activities, making it an important compound in the field of medicinal chemistry. This suggests that it may have therapeutic or other beneficial effects when used in the development of new drugs or treatments.
Explanation
The solubility of the compound in different solvents is not mentioned in the provided material. Solubility is an important property for determining the compound's reactivity and its potential use in various applications.
Explanation
The stability of the compound under different conditions (e.g., temperature, pH, etc.) is not mentioned in the provided material. Stability is an important factor to consider when evaluating the compound's suitability for various applications and its potential reactivity with other substances.
Structure
1,2,4-Triazin-3(2H)-one, 4-amino-4,5-dihydro-6-methyl-
Functional Groups
Triazine ring, amino group, and methyl group
Applications
Pharmaceutical and agrochemical synthesis, organic chemistry, and medicinal chemistry
Biological Activity
Potential pharmacological and biological activities
Solubility
Not specified in the provided material
Stability
Not specified in the provided material
Check Digit Verification of cas no
The CAS Registry Mumber 123313-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,3,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123313-07:
(8*1)+(7*2)+(6*3)+(5*3)+(4*1)+(3*3)+(2*0)+(1*7)=75
75 % 10 = 5
So 123313-07-5 is a valid CAS Registry Number.
123313-07-5Relevant articles and documents
Electrochemical versus anionic oxygenation of azathymine derivatives
Butora, Gabor,Reed, Josephine W.,Hudlicky, Tomas,Brammer Jr., Larry E.,Higgs, Paul I.,Simmons, Dana P.,Heard, Nina E.
, p. 7694 - 7701 (1997)
Pymetrozine (1) was converted to hemiaminal 2 in low to moderate yield by trapping its dianion with oxygen followed by reduction with ferrous salts. Pymetrozines 18 and 19 failed to undergo this type of oxygenation. All three pymetrozines were oxidized electrochemically at C5 to methyl hemiaminals 20, 21, and 22, respectively. Hydrolysis of 20 to 2 was accomplished under either acid- or base-catalyzed conditions in excellent yields, whereas the hydrolysis of methyl hemiaminals 21 and 22 was best performed under basic conditions. Soil metabolites of pymetrozine 1, hemiaminals 2 and 3, were prepared on a medium scale and in excellent yields. Linear sweep voltammetry data and conditions for preparative-scale electrochemistry are furnished for the precursory pymetrozines. Complete experimental and spectral data are provided for all new compounds, and the relative merits of anionic versus electrochemical oxidations for alkyl amides are discussed. A cautionary note is provided with the description of the conditions for large-scale anionic oxygenation because of potential explosive hazards.
