108905-65-3 Usage
Chemical structure
A complex structure with multiple functional groups and heteroatoms.
Bromo group
A bromine atom attached to the imidazole ring, which may influence the compound's reactivity and properties.
Methyl group
A small alkyl group attached to the imidazole ring, which can affect the compound's steric properties and reactivity.
Methylsulfanyl group
A sulfur-containing group attached to the imidazole ring, which may contribute to the compound's odor, reactivity, and potential biological activity.
Imidazole ring
A five-membered aromatic ring with two nitrogen atoms, which can participate in various chemical reactions and may be involved in biological activity.
Methylpyrazin-2-yl group
A pyrazine derivative with a methyl group attached to the 5-position, which may influence the compound's reactivity and properties.
Ethanol backbone
A hydroxyl group attached to an ethyl group, which can participate in hydrogen bonding and may influence the compound's solubility and reactivity.
Potential applications
Possible uses in pharmaceuticals, agrochemicals, or materials science due to its complex structure and potential biological activity.
Biological activity
May have antimicrobial or antifungal properties, but further research is needed to confirm these activities and understand the compound's full potential.
Further research
More studies are required to fully understand the properties, potential uses, and safety of this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 108905-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,9,0 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 108905-65:
(8*1)+(7*0)+(6*8)+(5*9)+(4*0)+(3*5)+(2*6)+(1*5)=133
133 % 10 = 3
So 108905-65-3 is a valid CAS Registry Number.
108905-65-3Relevant academic research and scientific papers
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.
