20662-93-5 Usage
Description
5-BROMO-2-METHYL-4-PHENYL-1,3-OXAZOLE is a heterocyclic chemical compound characterized by a molecular formula of C10H8BrNO and a molecular weight of 236.08 g/mol. It features a five-membered ring structure with oxygen and nitrogen atoms, and a bromo and methyl substituent along with a phenyl group. 5-BROMO-2-METHYL-4-PHENYL-1,3-OXAZOLE is widely recognized for its applications in organic synthesis and medicinal chemistry, where it serves as a versatile building block for the creation of pharmaceuticals and biologically active molecules. Its potential extends to agricultural chemicals and materials science, with ongoing research to explore its biological activities and pharmacological properties further.
Uses
Used in Organic Synthesis:
5-BROMO-2-METHYL-4-PHENYL-1,3-OXAZOLE is utilized as a key intermediate in organic synthesis for the preparation of a variety of complex organic molecules. Its unique structure allows for the formation of diverse chemical entities through various synthetic routes.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 5-BROMO-2-METHYL-4-PHENYL-1,3-OXAZOLE is employed as a building block for the synthesis of pharmaceuticals. Its incorporation into drug molecules can potentially enhance their therapeutic effects and pharmacological profiles.
Used in Agricultural Chemicals:
5-BROMO-2-METHYL-4-PHENYL-1,3-OXAZOLE may find applications in the development of agricultural chemicals, where its chemical properties could be harnessed to create novel pesticides or herbicides.
Used in Materials Science:
5-BROMO-2-METHYL-4-PHENYL-1,3-OXAZOLE's potential in materials science is being explored for its possible use in the development of new materials with unique properties, such as high thermal stability or specific electronic characteristics.
Used in Biological Research:
5-BROMO-2-METHYL-4-PHENYL-1,3-OXAZOLE is also used in biological research to study its interactions with biological systems. This research may uncover new biological activities and pharmacological properties, expanding its applications in therapeutic and diagnostic areas.
Check Digit Verification of cas no
The CAS Registry Mumber 20662-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,6,6 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 20662-93:
(7*2)+(6*0)+(5*6)+(4*6)+(3*2)+(2*9)+(1*3)=95
95 % 10 = 5
So 20662-93-5 is a valid CAS Registry Number.
20662-93-5Relevant articles and documents
Iodine(III)-Catalyzed Formal [2 + 2 + 1] Cycloaddition Reaction for Metal-Free Construction of Oxazoles
Yagyu, Takuma,Takemoto, Yusuke,Yoshimura, Akira,Zhdankin, Viktor V.,Saito, Akio
supporting information, p. 2506 - 2509 (2017/05/24)
The iodine(III) catalyst, in situ generated from iodoarene as a precatalyst with m-CPBA and Tf2NH, promoted the metal-free [2 + 2 + 1] cycloaddition-type reactions of alkynes, nitriles, and oxygen atoms for the regioselective formations of 2,4-disubstituted and 2,4,5-trisubstituted oxazole. A first example of iodine catalysis for multicomponent reactions is represented.
Synthesis of nitrooxazoles
Hammar,Rustad
, p. 885 - 888 (2007/10/02)
-
