120375-14-6 Usage
Description
4-(2-ETHYL-6-METHYLPHENYL)-5-METHYL-3-MORPHOLINONE, also known as a morpholine derivative, is a compound characterized by the presence of a morpholin-3-one structure substituted with a 2-ethyl-6-methylphenyl group at position 4 and a methyl group at position 5. It is identified as a metabolite of metolachlor, which is a widely used herbicide.
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 articles and documents
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
