33105-96-3 Usage
Uses
Used in Pharmaceutical Industry:
C-(2-P-TOLYL-OXAZOL-4-YL)-METHYLAMINE is used as a building block for the synthesis of pharmaceuticals due to its unique electronic and steric properties, which contribute to the development of novel drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, C-(2-P-TOLYL-OXAZOL-4-YL)-METHYLAMINE is utilized as a key intermediate in the creation of new agrochemicals, potentially leading to more effective and environmentally friendly pesticides and other agricultural products.
Used in Dye Industry:
C-(2-P-TOLYL-OXAZOL-4-YL)-METHYLAMINE is employed as a component in the production of dyes, where its chemical structure allows for the development of dyes with specific color properties and improved stability.
Used in Material Science:
C-(2-P-TOLYL-OXAZOL-4-YL)-METHYLAMINE is also used in material science as an intermediate for creating materials with tailored properties, such as improved conductivity, stability, or specific interactions with other molecules, which can be applied in various high-tech applications.
Check Digit Verification of cas no
The CAS Registry Mumber 33105-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,0 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33105-96:
(7*3)+(6*3)+(5*1)+(4*0)+(3*5)+(2*9)+(1*6)=83
83 % 10 = 3
So 33105-96-3 is a valid CAS Registry Number.
33105-96-3Relevant academic research and scientific papers
Design, Synthesis and Biological Evaluation of N-((2-phenyloxazol-4-yl)methyl) Pyrimidine Carboxamide Derivatives as Potential Fungicidal Agents
Huang, Danling,Zheng, Shumin,Cheng, Yong-Xian
, p. 185 - 191 (2021/02/12)
Twelve N-((2-phenyloxazol-4-yl)methyl) pyrimidine carboxamide derivatives were designed, synthesized, and characterized by 1H NMR, 13C NMR, and HRMS. The fungicidal activities of these new compounds against Sclerotinia sclerotiorum, Botrytis cinereal, and Colletotrichum fragariae were evaluated. The results indicated that compounds 5b, 5f, and 5g displayed potential fungicidal activities against tested fungi, especially 5f exhibited IC50 value of 28.9 mg/L against S. sclerotiorum. Moreover, the compounds 5f and 5g showed IC50 values of 54.8 mg/L and 62.2 mg/L against C. fragariae respectively, which shows that they were more active than the commercial fungicide hymexazol. The superficial structure-activity relationships were discussed, which may be of benefit for the development of fungicides and discovery of novel fungicides.
