172168-03-5 Usage
Description
4-[(4-Methoxyphenyl)methyl]-4-methyl-2-phenyl-5(4H)-oxazolone, with the CAS number 172168-03-5, is a white solid compound that is primarily utilized in the field of organic synthesis. It is a derivative of oxazolone, which is a heterocyclic compound known for its diverse applications in chemical reactions and the formation of various organic compounds.
Uses
Used in Organic Synthesis:
4-[(4-Methoxyphenyl)methyl]-4-methyl-2-phenyl-5(4H)-oxazolone is used as a synthetic building block for the creation of more complex organic molecules. Its unique structure allows it to participate in various chemical reactions, such as condensation, substitution, and addition reactions, leading to the formation of a wide range of organic compounds with different functionalities and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-[(4-Methoxyphenyl)methyl]-4-methyl-2-phenyl-5(4H)-oxazolone is used as a key intermediate in the synthesis of various drug molecules. Its ability to form diverse organic compounds makes it a valuable asset in the development of new drugs with potential therapeutic applications.
Used in Chemical Research:
4-[(4-Methoxyphenyl)methyl]-4-methyl-2-phenyl-5(4H)-oxazolone is also used in chemical research to study the reactivity and properties of oxazolone derivatives. Researchers can use this compound to explore new reaction pathways, develop innovative synthetic strategies, and gain a deeper understanding of the chemical behavior of similar compounds.
Used in Material Science:
In the field of material science, 4-[(4-Methoxyphenyl)methyl]-4-methyl-2-phenyl-5(4H)-oxazolone can be employed as a component in the development of novel materials with specific properties. Its incorporation into polymers, for example, can lead to materials with enhanced mechanical, thermal, or electrical properties, depending on the desired application.
Check Digit Verification of cas no
The CAS Registry Mumber 172168-03-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,1,6 and 8 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 172168-03:
(8*1)+(7*7)+(6*2)+(5*1)+(4*6)+(3*8)+(2*0)+(1*3)=125
125 % 10 = 5
So 172168-03-5 is a valid CAS Registry Number.
172168-03-5Relevant articles and documents
BEMP-promoted C(4)-alkylation of 4-alkyloxazol-5(4 H)-ones: A rapid and efficient route to α,α-dialkyl-α-amino acids
Lee, Yeon-Ju,Seo, Jeyoung,Kim, Dong-Guk,Park, Hyeung-Geun,Jeong, Byeong-Seon
, p. 701 - 704 (2013/05/09)
Rapid and efficient C(4)-alkylation of 4-alkyloxazol-5(4H)-ones has been achieved by the utilization of BEMP as base. 4,4-Dialkyloxazol-5(4H)-ones, which can easily be hydrolyzed into free α,α-dialkyl-α-amino acids, were obtained in high yields (up to 99%
