The chemical compound "2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,12,12a-hexahydro-3,5,10,11,12a-pentahydroxy-6-methyl-1,12-dioxo-,(4S,4aR,5R,12aS)-" is a complex organic molecule with a unique structure. It features a naphthacene core, which is a type of polycyclic aromatic hydrocarbon, and is further modified with various functional groups. The compound has a hexahydro ring system, indicating the presence of six hydrogen atoms in a cyclic structure. It also contains five hydroxyl groups, which are alcohol-like groups capable of forming hydrogen bonds, and one dimethylamino group, contributing to its basic character. The molecule is chiral, with the stereochemistry specified by the (4S,4aR,5R,12aS) notation, indicating the specific three-dimensional arrangement of atoms around the chiral centers. 2-Naphthacenecarboxamide,4-(dimethylamino)- 1,4,4a,5,12,12a-hexahydro-3,5,10,11,12a-pentahydroxy- 6-methyl-1,12-dioxo-,(4S,4aR,5R,- 12aS)- is characterized by its 6-methyl group and two oxo groups, which are carbonyl groups that contribute to its reactivity and stability. Overall, this chemical is a highly functionalized and stereospecific molecule with potential applications in various fields, such as pharmaceuticals or materials science, due to its intricate structure and properties.
The CAS Registry Mumber 4660-26-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 0 respectively; the second part has 2 digits, 2 and 6 respectively. Calculate Digit Verification of CAS Registry Number 4660-26: (6*4)+(5*6)+(4*6)+(3*0)+(2*2)+(1*6)=88 88 % 10 = 8 So 4660-26-8 is a valid CAS Registry Number.
4660-26-8SDS
SAFETY DATA SHEETS
According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition
Shang, Zhuo,Salim, Angela A.,Khalil, Zeinab,Quezada, Michelle,Bernhardt, Paul V.,Capon, Robert J.
, p. 12501 - 12508 (2015)
Viridicatumtoxins, which belong to a rare class of fungal tetracycline-like mycotoxins, were subjected to comprehensive spectroscopic and chemical analysis, leading to reassignment/assignment of absolute configurations and characterization of a remarkably
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