138336-09-1 Usage
Molecular Structure
2-[2-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)prop-2-en-1-yl]-6-methylpyrazine is a derivative of pyrazine, a bicyclic organic compound consisting of two six-membered nitrogen-containing rings (azine) fused together. The compound contains a 2,4-dibromo-1-methyl-1H-imidazol-5-yl group and a prop-2-en-1-yl group attached to the pyrazine ring.
Functional Groups
The compound contains several functional groups, including two bromine atoms, a methyl group, and a prop-2-en-1-yl group.
Physical Properties
The physical properties of 2-[2-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)prop-2-en-1-yl]-6-methylpyrazine are not provided in the material.
Uses
The compound is used in various industries, including pharmaceutical, agricultural, and chemical manufacturing. It may have applications as a building block in organic synthesis, as well as potential uses in the development of new drugs, agrochemicals, and other chemical products.
Biological Activities
2-[2-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)prop-2-en-1-yl]-6-methylpyrazine has potential biological activities and may be of interest for further research and development.
Safety Profile
The safety profile of 2-[2-(2,4-dibromo-1-methyl-1H-imidazol-5-yl)prop-2-en-1-yl]-6-methylpyrazine is not provided in the material. However, due to the presence of bromine atoms and other functional groups, it may pose potential health risks and appropriate safety precautions should be taken when handling the compound.
Check Digit Verification of cas no
The CAS Registry Mumber 138336-09-1 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 9 respectively.
Calculate Digit Verification of CAS Registry Number 138336-09:
(8*1)+(7*3)+(6*8)+(5*3)+(4*3)+(3*6)+(2*0)+(1*9)=131
131 % 10 = 1
So 138336-09-1 is a valid CAS Registry Number.
138336-09-1Relevant 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.
