1173666-68-6 Usage
Description
(R)-Methyl-6'-hydroxy-8a'-methyl-3',4',4a',5',8',8a'-hexahydro-2'H-spiro[1,3-dioxolane-2,1'-naphthalene]-7'-carboxylate is a complex organic chemical compound characterized by a unique spiro scaffold. It features a naphthalene core fused with a 2'H-spiro[1,3-dioxolane-2,1'] ring system and a carboxylate functional group. (R)-Methyl-6'-hydroxy-8a'-methyl-3',4',4a',5',8',8a'-hexahydro-2'H-spiro[1,3-dioxolane-2,1'-naphthalene]-7'-carboxylate also includes a methyl group at the 6' position, a hydroxy group at the 8a' position, and another methyl group at the 8' position. As a member of the carboxylic acid esters class, it holds potential for various applications in organic synthesis, pharmaceuticals, and medicinal chemistry, with its specific properties making it a subject of interest for further research and development.
Uses
Used in Organic Synthesis:
(R)-Methyl-6'-hydroxy-8a'-methyl-3',4',4a',5',8',8a'-hexahydro-2'H-spiro[1,3-dioxolane-2,1'-naphthalene]-7'-carboxylate is used as an intermediate in organic synthesis for the creation of more complex molecules due to its unique structural features and reactivity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (R)-Methyl-6'-hydroxy-8a'-methyl-3',4',4a',5',8',8a'-hexahydro-2'H-spiro[1,3-dioxolane-2,1'-naphthalene]-7'-carboxylate is used as a building block for the development of novel drugs, potentially targeting specific biological receptors or pathways due to its intricate structure and functional groups.
Used in Medicinal Chemistry:
(R)-Methyl-6'-hydroxy-8a'-methyl-3',4',4a',5',8',8a'-hexahydro-2'H-spiro[1,3-dioxolane-2,1'-naphthalene]-7'-carboxylate serves as a key component in medicinal chemistry for the design and synthesis of new therapeutic agents, possibly owing to its ability to modulate biological targets or its potential to be modified for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1173666-68-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,3,6,6 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1173666-68:
(9*1)+(8*1)+(7*7)+(6*3)+(5*6)+(4*6)+(3*6)+(2*6)+(1*8)=176
176 % 10 = 6
So 1173666-68-6 is a valid CAS Registry Number.
1173666-68-6Relevant articles and documents
Effect of C-9 Substituents on the Regioselectivity of A-Ring Reactions in Derivatives of the Wieland-Miescher Ketone
Park, Kwangyong,Scott, William J.,Wiemer, David F.
, p. 6313 - 6317 (2007/10/02)
The nature of C-9 substituents was found to have a significant influence on the regio- and stereochemistry of A-ring reactions in a variety of Wieland-Miescher ketone derivatives.For example, Pd-catalyzed hydrogenation of the C-9 dioxolanes resulted in much better selectivity for the cis-fused products vis-a-vis the corresponding C-9 ketone, with the parent Wieland-Miescher ketone itself and both C-4 methyl and C-4 carboalkoxy substituted analogues.In addition, methylation and acylation of A-ring enolates favored the C-2 isomer when a C-9 dioxolane group was present, but the C-4 substituted isomer was predominant with the corresponding C-9 ketone.These differences in regiochemistry may allow selective elaboration of cis-fused decalins during preparation of complex natural products.
