2-[[(Aminothioxomethyl)amino]carbonyl]-2-ethyl-3-methylhexanoic acid, identified by its CAS number 93227-84-0, is a synthetic organic compound characterized by its complex structure, which includes an amino group, a thioxo moiety, and a carboxylic acid functional group. This compound typically exhibits properties associated with amino acids, such as being polar and capable of forming hydrogen bonds, which can influence its solubility in water and organic solvents. The presence of the thioxo group may impart unique reactivity and stability characteristics, potentially making it useful in various chemical applications, including pharmaceuticals or agrochemicals. Its molecular structure suggests it may participate in biological processes or act as a precursor in synthetic pathways. Additionally, the branched alkyl chains contribute to its hydrophobic characteristics, which can affect its interaction with biological membranes. Overall, the compound's specific properties, such as melting point, boiling point, and reactivity, would require empirical measurement or detailed computational analysis for precise characterization.

2-[[(AMinothioxoMethyl)aMino]carbonyl]-2-ethyl-3-Methylhexanoic Acid

93227-84-0: 2-[[(Aminothioxomethyl)amino]carbonyl]-2-ethyl-3-methylhexanoic acid, identified by its CAS number 93227-84-0, is a synthetic organic compound characterized by its complex structure, which includes an amino group, a thioxo moiety, and a carboxylic acid functional group. This compound typically exhibits properties associated with amino acids, such as being polar and capable of forming hydrogen bonds, which can influence its solubility in water and organic solvents. The presence of the thioxo group may impart unique reactivity and stability characteristics, potentially making it useful in various chemical applications, including pharmaceuticals or agrochemicals. Its molecular structure suggests it may participate in biological processes or act as a precursor in synthetic pathways. Additionally, the branched alkyl chains contribute to its hydrophobic characteristics, which can affect its interaction with biological membranes. Overall, the compound's specific properties, such as melting point, boiling point, and reactivity, would require empirical measurement or detailed computational analysis for precise characterization.

CAS 93227-84-0

2-[[(AMinothioxoMethyl)aMino]carbonyl]-2-ethyl-3-Methylhexanoic Acid

Thiopental EP Impurity D

Ref: ST-EA-CP-T202004