138336-00-2 Usage
Chemical structure
2-[(1E)-2-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)prop-1-en-1-yl]-5-methylpyrazine A pyrazine derivative containing a dibromo-substituted imidazole group and a methylpyrazine group.
Type of compound
Pyrazine derivative A chemical compound derived from pyrazine, which is a heterocyclic organic compound with the formula C4H4N2.
Common uses
Synthesis of pharmaceuticals and agrochemicals This compound is frequently utilized as a building block or intermediate in the production of various drugs and agricultural chemicals.
Potential biological activities
Antifungal and antimicrobial properties The compound has been studied for its ability to inhibit the growth of fungi and microorganisms, which could be useful in the development of new treatments for infections.
Possible applications
Development of new materials and organic electronic devices Due to its unique chemical structure and properties, 2-[(1E)-2-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)prop-1-en-1-yl]-5-methylpyrazine may be employed in the creation of innovative materials and technologies in the field of organic electronics.
Check Digit Verification of cas no
The CAS Registry Mumber 138336-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,3 and 6 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138336-00:
(8*1)+(7*3)+(6*8)+(5*3)+(4*3)+(3*6)+(2*0)+(1*0)=122
122 % 10 = 2
So 138336-00-2 is a valid CAS Registry Number.
138336-00-2Relevant articles and documents
Regiospecific Synthesis of the Aminoimidazoquinoxaline (IQx) Mutagens from Cooked Foods
Bierer, Donald E.,O'Connell, John F.,Parquette, Jon R.,Thompson, Charles M.,Rapoport, Henry
, p. 1390 - 1405 (2007/10/02)
A versatile regiospecific synthesis has been developed to prepare the six dimethyl- and trimethyl-substituted 2-aminoimidazoquinoxaline (IQx) regioisomers 35, 36, 37, 38, 39, and 40 for complete and unambiguous characterization.The key reaction step in the synthetic sequence for these angular tricycles is a photodehydrohalogenative cyclization of suitably substituted pyrazinylimidazolylethylene intermediates derived from common pyrazine and fully functionalized imidazole precursors.The reaction sequence developed allows for versatility in the substitution pattern as well as total regioisomeric control for the synthesis of all possible methyl and polymethyl analogues of IQx.Comparison of the physical properties among the isomeric di- and trimethyl-IQx's has established the value of unambiguous regiospecific synthesis for structural assignments in this food mutagen series.