130403-23-5 Usage
Description
3-[(2,6-dimethylphenyl)carbamoyl]isoxazol-5-ylmethyl acetate is a chemical compound characterized by its unique molecular structure, featuring a five-membered aromatic heterocyclic isoxazole ring with a methyl acetate group and a carbamoyl group attached. The carbamoyl group is composed of a phenyl ring substituted with two methyl groups. 3-[(2,6-dimethylphenyl)carbamoyl]isoxazol-5-ylmethyl acetate, with the molecular formula C14H16N2O4, exhibits potential for diverse chemical and biological activities, making it a valuable compound for further research and development in various fields.
Uses
Used in Pharmaceutical Applications:
3-[(2,6-dimethylphenyl)carbamoyl]isoxazol-5-ylmethyl acetate is used as a building block for the development of new pharmaceutical compounds due to its unique structural and functional properties. Its potential for diverse chemical and biological activities allows for the creation of novel drugs with specific therapeutic targets.
Used in Agrochemical Applications:
In the agrochemical industry, 3-[(2,6-dimethylphenyl)carbamoyl]isoxazol-5-ylmethyl acetate is used as a starting material for the synthesis of various agrochemicals, such as pesticides and herbicides. Its structural diversity enables the development of targeted and effective compounds for crop protection and management.
Used in Material Sciences:
3-[(2,6-dimethylphenyl)carbamoyl]isoxazol-5-ylmethyl acetate is utilized as a key component in the development of advanced materials for various applications, including electronics, coatings, and adhesives. Its unique properties contribute to the creation of materials with enhanced performance characteristics, such as improved stability, durability, and functionality.
Overall, 3-[(2,6-dimethylphenyl)carbamoyl]isoxazol-5-ylmethyl acetate is a versatile compound with a wide range of potential applications across different industries, making it a valuable asset for ongoing research and development efforts.
Check Digit Verification of cas no
The CAS Registry Mumber 130403-23-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,4,0 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130403-23:
(8*1)+(7*3)+(6*0)+(5*4)+(4*0)+(3*3)+(2*2)+(1*3)=65
65 % 10 = 5
So 130403-23-5 is a valid CAS Registry Number.
130403-23-5Relevant articles and documents
N(pyrazol-3-yl) benzamides and pharmaceutical compositions
-
, (2008/06/13)
The invention relates to a compound useful for treating epilepsy selected from the compounds of the general formula: STR1 in which R1 is C1 -C4 alkyl, R2 is C1 -C4 alkyl, R3 is selected from hydrogen, C1 -C4 alkyl, C1 -C4 alkoxy and C1 -C4 hydroxyalkyl, and R4 is selected from hydrogen, C1 -C4 alkyl, C2 -C7 alkanoyl and C1 -C4 hydroxyalkyl.
New N-aryl isoxazolecarboxamides and N-isoxazolylbenzamides as anticonvulsant agents
Lepage,Tombret,Cuvier,Marivain,Gillardin
, p. 581 - 593 (2007/10/02)
We prepared a series of N-aryl isoxazolecarboxamide, N-isoxazolylbenzamide compounds and derivatives and studied their anticonvulsant action in MES and MMS tests. Some of these reveal considerable activity, especially with respect to MES test. The disubstitution in the 2.6-position on the phenyl ring by two methyl groups would appear to be of primary importance for the activity. The amide bridge between the phenyl and isoxazolic rings, whether of the anilide or benzamide type, seems to show similar anticonvulsant behavior. We have selected the derivatives 8 (N-(2.6-dimethylphenyl)-5-methyl-3-isoxazolecarboxamide, 12 (N-(2.6-dimethylphenyl)-5-hydroxymethyl-3-isoxazolecarboxamide) and 51 (N-(5-methyl-3-isoxazolyl)-2.6-dimethylbenzamide) which are presently being studied in more extended pharmacological tests.
