120375-14-6 Usage
Uses
Used in Pharmaceutical Industry:
4-(2-ETHYL-6-METHYLPHENYL)-5-METHYL-3-MORPHOLINONE is used as an intermediate compound for the synthesis of various pharmaceutical products. Its unique chemical structure allows it to be a valuable building block in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Chemical Research:
In the field of chemical research, 4-(2-ETHYL-6-METHYLPHENYL)-5-METHYL-3-MORPHOLINONE serves as a key compound for studying the properties and reactivity of morpholine derivatives. This can lead to a better understanding of their potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Environmental Monitoring:
As a metabolite of metolachlor, 4-(2-ETHYL-6-METHYLPHENYL)-5-METHYL-3-MORPHOLINONE can be used in environmental monitoring and assessment programs. Its detection and quantification in soil, water, and plant samples can provide valuable information on the fate and behavior of metolachlor in the environment, as well as its potential impact on ecosystems and human health.
Used in Analytical Chemistry:
The unique chemical structure of 4-(2-ETHYL-6-METHYLPHENYL)-5-METHYL-3-MORPHOLINONE makes it a useful reference compound in analytical chemistry. It can be employed as a standard or calibration material for the development and validation of analytical methods, such as chromatography, mass spectrometry, and spectroscopy, which are crucial for the accurate identification and quantification of similar compounds in complex samples.
Check Digit Verification of cas no
The CAS Registry Mumber 120375-14-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,7 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120375-14:
(8*1)+(7*2)+(6*0)+(5*3)+(4*7)+(3*5)+(2*1)+(1*4)=86
86 % 10 = 6
So 120375-14-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H19NO2/c1-4-12-7-5-6-10(2)14(12)15-11(3)8-17-9-13(15)16/h5-7,11H,4,8-9H2,1-3H3
120375-14-6Relevant academic research and scientific papers
Participation of neighbouring amide group in the competitive acid catalysed hydrolysis of ether linkage and an intramolecular S(N)2 reactions. 2
Arcelli, Antonio,Papa, Matteo,Porzi, Gianni,Sandri, Sergio
, p. 10513 - 10516 (2007/10/03)
The substrate 1 was submitted to acid hydrolysis and two reaction products (2,3) were obtained in competitive reactions (a parallel pathway). The experimental data, elaborated by using the expressions for the parallel first-order reactions, showed the for
Photodegradation of Metolachlor in Water in the Presence of Soil Mineral and Organic Constituents
Mathew, Regi,Khan, Shahamat U.
, p. 3996 - 4000 (2007/10/03)
Photodegradation of metolachlor [2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)-acetamide] at 253.7 nm was carried out in water containing soil minerals (kaolinite, montmorillonite, and goethite) and fulvic acid under two different pH conditions. The rate of photolysis was dependent on the nature of the soil constituents and the initial pH of the medium. Based on the regression analysis, it was shown that the photodegradation followed the first-order kinetics with respect to the metolachlor concentration, and the half-life of the herbicide under UV irradiation was longer in the absence of soil constituents. Hydroxylation, dehalogenation, oxoquinoline formation, and demethylation were the main processes observed during the photolysis of metolachlor. More degradation products were formed in the presence of kaolinite, montmorillonite, and goethite than with fulvic acid and water alone. The major degradation product formed under UV irradiation in all the treatments was identified as 4-(2-ethyl-6-methylphenyl)-5-methyl-3-morpholine.
