6826-26-2 Usage
Uses
Used in Research Applications:
5-(4-Bromophenyl)oxazol-2-amine is used as a research chemical for the development and study of new compounds and materials. Its unique structure and properties make it a valuable tool in the field of organic chemistry and drug discovery.
Used in Pharmaceutical Applications:
5-(4-Bromophenyl)oxazol-2-amine is used as an intermediate in the synthesis of pharmaceutical compounds. Its potential biological activities and versatile chemical structure make it a promising candidate for the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
5-(4-Bromophenyl)oxazol-2-amine is used as a building block in the synthesis of various organic compounds. Its reactivity and functional groups allow for the formation of a wide range of chemical products, making it a valuable component in the chemical industry.
Used in Material Science:
5-(4-Bromophenyl)oxazol-2-amine may have potential applications in the development of new materials with unique properties. Its chemical structure and reactivity could contribute to the creation of advanced materials for various industries, such as electronics, coatings, and polymers.
Used in Environmental Applications:
5-(4-Bromophenyl)oxazol-2-amine may also have potential uses in environmental applications, such as the development of new methods for pollution control or the creation of environmentally friendly materials. Its unique properties and reactivity could contribute to the development of innovative solutions for environmental challenges.
Check Digit Verification of cas no
The CAS Registry Mumber 6826-26-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,2 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6826-26:
(6*6)+(5*8)+(4*2)+(3*6)+(2*2)+(1*6)=112
112 % 10 = 2
So 6826-26-2 is a valid CAS Registry Number.
6826-26-2Relevant academic research and scientific papers
Novel and efficient synthesis of 2-aminooxazoles from pyrimidin-2(1H)-one
Alifanov, Vadim L.,Babaev, Eugene V.
, p. 263 - 270 (2007/10/03)
Stepwise conversion of pyrimidin-2(1H)-one to 2-amino-5-aryloxazoles via oxazolo[3,2-a]pyrimidinium salts is reported. The sequence involves, (i) regioselective N-alkylation of pyrimidone by phenacyl bromides, (ii) cyclization of obtained 1-(2-aryl-2-oxoethyl)pyrimidin-2(1H)-ones into oxazolo[3,2-a] pyrimidinium salts under the action of fuming sulfuric (or triflic) acid, and (iii) reaction of the obtained salts with hydrazine leading to 2-amino-5-aryloxazoles. Georg Thieme Verlag Stuttgart.
