630059-96-0 Usage
Molecular structure
The compound has a complex molecular structure consisting of a 1,4-dioxa ring, a thiadispiro ring, and a phenyl group.
Classification
It is classified as a cyclohexanone derivative.
Chirality
The compound is chiral, meaning it has a specific orientation of its three-dimensional structure.
Stereochemistry
The stereochemistry of the compound is (3R,5R,6S)-, indicating the specific arrangement of atoms in the molecule.
Potential applications
It is likely used in organic synthesis and chemical research, but its applications and characteristics would require further analysis and investigation.
Functional groups
The compound contains a carbonyl group (C=O) and a phenyl group (C6H5).
Ring systems
It has two ring systems a 1,4-dioxa ring and a thiadispiro ring.
Aromaticity
The phenyl group in the compound is aromatic, which contributes to its stability and reactivity.
Stereoisomers
Due to its chirality, the compound has stereoisomers, which are molecules with the same molecular formula but different spatial arrangements of atoms.
Solubility
The compound's solubility properties would depend on its polarity and molecular structure, which could be influenced by the presence of the carbonyl group and the phenyl group.
Check Digit Verification of cas no
The CAS Registry Mumber 630059-96-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,0,0,5 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 630059-96:
(8*6)+(7*3)+(6*0)+(5*0)+(4*5)+(3*9)+(2*9)+(1*6)=140
140 % 10 = 0
So 630059-96-0 is a valid CAS Registry Number.
630059-96-0Relevant academic research and scientific papers
C4'-spiroalkylated nucleosides having sulfur incorporated at the apex position.
Paquette, Leo A,Fabris, Fabrizio,Gallou, Fabrice,Dong, Shuzhi
, p. 8625 - 8634 (2007/10/03)
Methodology based on the concept of thionium ion-initiated pinacolic ring expansion has been developed for accessing C4'-spirocyclic thionucleosides. The readily available racemic ketones 6 and 37 are conveniently resolved via their acetals with (R)-mandelic acid. Subsequent reactions beginning with utilization of the Pummerer rearrangement lend themselves to functionalization of the spirocyclic core and ultimately incorporation of the nucleosidic bases. Limitations to this strategy are pointed out. Acquisition of the alpha- and beta-isomers at C4' is equally facile. Absolute configurational assignments have been made possible by X-ray crystallography.
