169310-98-9 Usage
Uses
Used in Pharmaceutical Development:
Isoxazole, 4-bromo-3-ethoxy-5-methylis used as a building block in pharmaceutical development for the synthesis of various organic compounds and potential drug candidates. Its unique structure and properties contribute to the discovery and development of new therapeutic agents.
Used in Chemical Research:
Isoxazole, 4-bromo-3-ethoxy-5-methylis utilized in chemical research to study its properties and potential applications. Its unique structure makes it an important target for chemical synthesis and investigation, furthering the understanding of isoxazole-based compounds and their potential uses in various fields.
Used in Organic Synthesis:
Isoxazole, 4-bromo-3-ethoxy-5-methylis employed as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its versatile structure allows for the formation of diverse chemical entities, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
Isoxazole, 4-bromo-3-ethoxy-5-methylis applied in medicinal chemistry for the design and synthesis of novel bioactive molecules. Its unique structural features enable the development of compounds with potential therapeutic applications, contributing to the advancement of drug discovery and the treatment of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 169310-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,3,1 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 169310-98:
(8*1)+(7*6)+(6*9)+(5*3)+(4*1)+(3*0)+(2*9)+(1*8)=149
149 % 10 = 9
So 169310-98-9 is a valid CAS Registry Number.
169310-98-9Relevant academic research and scientific papers
A convenient synthesis of 4-substituted 3-ethoxy-5-methylisoxazoles by palladium-catalyzed coupling reactions
Kromann, Hasse,Sl?k, Frank A,Johansen, Tommy N,Krogsgaard-Larsen, Povl
, p. 2195 - 2201 (2007/10/03)
The coupling reactions were performed using 3-ethoxy-4-iodo-5-methylisoxazole (4) as the key intermediate. Coupling of 4 under Suzuki-Miyaura or Stille conditions using Pd(PPh3)2Cl2 and arylboronic acids or aryltin analogu
