21354-98-3 Usage
Uses
Used in Pharmaceutical Research:
5-Bromo-4-methyl-2-phenyl-1,3-oxazole is utilized as a reagent in the development of pharmaceutical drugs due to its unique structure and reactivity. It serves as a building block for the synthesis of various biologically active compounds, contributing to the discovery of new therapeutic agents.
Used in Agrochemical Development:
5-BROMO-4-METHYL-2-PHENYL-1,3-OXAZOLE is also employed in the research and development of agrochemicals, where its properties can be harnessed to create effective and targeted solutions for agricultural applications.
Used in Organic Synthesis:
5-Bromo-4-methyl-2-phenyl-1,3-oxazole is used as an intermediate in organic synthesis, allowing for the creation of a wide range of chemical compounds. Its bromine substituent makes it a versatile precursor for further functionalization, expanding its utility in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-bromo-4-methyl-2-phenyl-1,3-oxazole is applied as a key component in the design and synthesis of novel drug candidates. Its unique structural features enable the development of compounds with potential therapeutic applications, advancing the discovery of new treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 21354-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,5 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21354-98:
(7*2)+(6*1)+(5*3)+(4*5)+(3*4)+(2*9)+(1*8)=93
93 % 10 = 3
So 21354-98-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H8BrNO/c1-7-9(11)13-10(12-7)8-5-3-2-4-6-8/h2-6H,1H3
21354-98-3Relevant academic research and scientific papers
Shibata, Katsunori,Kuroki, Lumi,Fukaminato, Tuyoshi,Irie, Masahiro
, p. 832 - 833 (2008)
A diarylethene derivative, in which oxazole rings are attached to the ethene moiety at the 5-position, was synthesized, and its photochromic and fluorescent properties were examined. The derivative undergoes photochromism in solution and the open-ring iso
Chemistry of 5-oxodihydroisoxazoles. Part 18. Synthesis of oxazoles by the photolysis and pyrolysis of 2-acyl-5-oxo-2,5-dihydroisoxazoles
Prager, Rolf H.,Smith, Jason A.,Weber, Ben,Williams, Craig M.
, p. 2665 - 2672 (2007/10/03)
N-Acylisoxazol-5-ones lose carbon dioxide under photochemical and thermal conditions affording iminocarbenes which undergo intramolecular cyclisation through the oxygen of the acyl group to give oxazoles. Under photochemical conditions those acylisoxazolones with electron withdrawing groups at C-4 usually give high yields of oxazoles, while those with electron donating groups at C-4 give only poor yields: the reverse is observed under thermal conditions.
