885272-89-9 Usage
Description
C-[2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHYLAMINE is a chemical compound that belongs to the class of oxazole derivatives. It features a central oxazole ring with a 4-fluoro-phenyl group and a methylamine group attached at the 2-position. C-[2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHYLAMINE is of interest in pharmaceutical and agrochemical industries, as well as in research due to its potential applications and the specific properties conferred by the fluorine substituent. The oxazole moiety is known for its bioactive properties, making it a valuable component in drug design and discovery.
Uses
Used in Pharmaceutical Industry:
C-[2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHYLAMINE is used as a potential active pharmaceutical ingredient for the development of new drugs. Its unique structure and the presence of the fluorine atom can contribute to specific biological activities and properties, making it a promising candidate for further investigation and development.
Used in Agrochemical Industry:
In the agrochemical industry, C-[2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHYLAMINE is used as a potential active ingredient in the development of new pesticides or herbicides. The oxazole moiety and the 4-fluoro-phenyl group may provide specific modes of action or selectivity against target pests or weeds.
Used in Research:
C-[2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHYLAMINE is used as a research compound for studying its chemical properties, reactivity, and potential applications in various fields. Its unique structure and the presence of the fluorine atom make it an interesting subject for exploration in synthetic chemistry, medicinal chemistry, and materials science.
Overall, C-[2-(4-FLUORO-PHENYL)-OXAZOL-4-YL]-METHYLAMINE is a compound with promising potential for various applications in the field of chemistry and life sciences, particularly in pharmaceutical and agrochemical industries, as well as in research. Its unique structure, the presence of the fluorine substituent, and the bioactive properties of the oxazole moiety make it a valuable compound for further investigation and development.
Check Digit Verification of cas no
The CAS Registry Mumber 885272-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 885272-89:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*2)+(2*8)+(1*9)=219
219 % 10 = 9
So 885272-89-9 is a valid CAS Registry Number.
885272-89-9Relevant articles and documents
COMPOUNDS AND METHODS for the inhibition of HDAC
-
Paragraph 0668-0669, (2015/11/24)
Disclosed are compounds having the formula: wherein X1, X2, X3, R1, R2, R3, R4, Y, A, Z, L and n are as defined herein, and methods of making and using the same.