460081-22-5 Usage
Description
Ethyl 2,5-dibroMo-1,3-oxazole-4-carboxylate is a chemical compound that belongs to the oxazole family. It is characterized by the presence of a bromine atom at the 2nd and 5th positions and a carboxylate group at the 4th position. Ethyl 2,5-dibroMo-1,3-oxazole-4-carboxylate is known for its unique chemical properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
Ethyl 2,5-dibroMo-1,3-oxazole-4-carboxylate is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
Ethyl 2,5-dibroMo-1,3-oxazole-4-carboxylate is used as a building block in the synthesis of substituted oxazoles. These substituted oxazoles can be further used in the development of various chemical products, including agrochemicals, dyes, and other specialty chemicals.
Used in Research and Development:
Ethyl 2,5-dibroMo-1,3-oxazole-4-carboxylate is also used in research and development laboratories for studying the properties and reactions of oxazole compounds. This helps in understanding their potential applications and developing new methods for their synthesis and modification.
Check Digit Verification of cas no
The CAS Registry Mumber 460081-22-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,0,0,8 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 460081-22:
(8*4)+(7*6)+(6*0)+(5*0)+(4*8)+(3*1)+(2*2)+(1*2)=115
115 % 10 = 5
So 460081-22-5 is a valid CAS Registry Number.
460081-22-5Relevant articles and documents
Ethyl 2-chlorooxazole-4-carboxylate: A versatile intermediate for the synthesis of substituted oxazoles
Hodgetts, Kevin J.,Kershaw, Mark T.
, p. 2905 - 2907 (2007/10/03)
(formula presented) R1 = Ar, Het, alkenyl R2 = H, Ar, Het, alkenyl, alkynyl R3 = H, CO2H, Ar, Het, alkenyl, alkynyl By using a sequence of regiocontrolled halogenation and palladium-catalyzed coupling reactions,
