Ammonium (Z)-amino[(4R,4aS,5aS,6S,12aS)-4-(dimethylamino)-6,10,11,12a-tetrahydroxy-6-methyl-1,3,12-trioxo-3,4,4a,5,5a,6,12,12a-octahydrotetracen-2(1H)-ylidene]methanolate, with CAS number 16505-45-6, is a complex organic compound characterized by its intricate molecular structure, which includes multiple hydroxyl groups and a dimethylamino functional group. This compound is likely to exhibit significant solubility in polar solvents due to the presence of hydroxyl groups, which can engage in hydrogen bonding. Its tetrahydroxy and trioxo functionalities suggest potential reactivity, making it a candidate for various chemical transformations. The stereochemistry indicated by the R and S designations implies that the compound may exhibit chirality, which can influence its biological activity and interactions. Additionally, the presence of a methanolate group suggests that it may participate in nucleophilic reactions. Overall, this compound's unique structural features may confer specific properties that could be of interest in fields such as medicinal chemistry or materials science.

ammonium (Z)-amino[(4R,4aS,5aS,6S,12aS)-4-(dimethylamino)-6,10,11,12a-tetrahydroxy-6-methyl-1,3,12-trioxo-3,4,4a,5,5a,6,12,12a-octahydrotetracen-2(1H)-ylidene]methanolate

16505-45-6: Ammonium (Z)-amino[(4R,4aS,5aS,6S,12aS)-4-(dimethylamino)-6,10,11,12a-tetrahydroxy-6-methyl-1,3,12-trioxo-3,4,4a,5,5a,6,12,12a-octahydrotetracen-2(1H)-ylidene]methanolate, with CAS number 16505-45-6, is a complex organic compound characterized by its intricate molecular structure, which includes multiple hydroxyl groups and a dimethylamino functional group. This compound is likely to exhibit significant solubility in polar solvents due to the presence of hydroxyl groups, which can engage in hydrogen bonding. Its tetrahydroxy and trioxo functionalities suggest potential reactivity, making it a candidate for various chemical transformations. The stereochemistry indicated by the R and S designations implies that the compound may exhibit chirality, which can influence its biological activity and interactions. Additionally, the presence of a methanolate group suggests that it may participate in nucleophilic reactions. Overall, this compound's unique structural features may confer specific properties that could be of interest in fields such as medicinal chemistry or materials science.

<p>4-Epitetracycline ammonium is a tetracycline analog, which is a derivative of the well-known antibiotic tetracycline. This compound is synthesized from naturally occurring tetracycline through chemical modification, involving the alteration of the hydroxyl group at the C-4 position. As a result, 4-Epitetracycline ammonium retains the fundamental characteristics of its parent compound.</p>

CAS 16505-45-6

ammonium (Z)-amino[(4R,4aS,5aS,6S,12aS)-4-(dimethylamino)-6,10,11,12a-tetrahydroxy-6-methyl-1,3,12-trioxo-3,4,4a,5,5a,6,12,12a-octahydrotetracen-2(1H)-ylidene]methanolate

4-Epitetracycline ammonium

Ref: 3D-RAA50545