885272-87-7

Basic information

• Product Name: C-[2-(4-METHOXY-PHENYL)-OXAZOL-4-YL]-METHYLAMINE
• Synonyms: C-[2-(4-METHOXY-PHENYL)-OXAZOL-4-YL]-METHYLAMINE;2-(4-methoxyphenyl)-4-Oxazolemethanamine;(2-(4-Methoxyphenyl)oxazol-4-yl)methanamine
• CAS NO: 885272-87-7
• Molecular Formula: C11H12N2O2
• Molecular Weight: 204.23
• Mol File: 885272-87-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: C-[2-(4-METHOXY-PHENYL)-OXAZOL-4-YL]-METHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: C-[2-(4-METHOXY-PHENYL)-OXAZOL-4-YL]-METHYLAMINE(885272-87-7)
• EPA Substance Registry System: C-[2-(4-METHOXY-PHENYL)-OXAZOL-4-YL]-METHYLAMINE(885272-87-7)

Safety Data

• Hazardous Substances Data: 885272-87-7(Hazardous Substances Data)

Usage

General Description

C-[2-(4-METHOXY-PHENYL)-OXAZOL-4-YL]-METHYLAMINE, also known as 4-Methoxyphenyl-2-oxazol-4-ylmethylamine, is a chemical compound with the molecular formula C11H13N2O2. It is a derivative of oxazole and is commonly used in the pharmaceutical and research industries. C-[2-(4-METHOXY-PHENYL)-OXAZOL-4-YL]-METHYLAMINE is of interest due to its potential to act as a ligand or substrate in various chemical and biological processes. Additionally, it may have applications in the development of new medications, particularly those related to the central nervous system. Further study of C-[2-(4-METHOXY-PHENYL)-OXAZOL-4-YL]-METHYLAMINE is needed to fully understand its properties and potential uses.

Upstream product

• 3424-93-9 4-methoxyphenylacetamide 
• 167155-56-8 4-(chloromethyl)-2-(4-methoxyphenyl)oxazole 
• 1074-82-4 potassium phtalimide 

Relevant articles and documents

Design, Synthesis and Biological Evaluation of N-((2-phenyloxazol-4-yl)methyl) Pyrimidine Carboxamide Derivatives as Potential Fungicidal Agents

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.