810682-41-8

Usage

Explanation

The compound is composed of 14 carbon atoms, 24 hydrogen atoms, and 2 oxygen atoms.
2. Spiroketone compound

Explanation

It is a type of chemical compound that contains a spiro ring system and a ketone functional group.
3. Bicyclic structure

Explanation

The compound has two fused rings, a seven-membered ring and a six-membered ring, forming a complex structure.
4. Chiral center

Explanation

The compound has a chiral center, which means it can exist in different stereoisomers (enantiomers).
5. (5S)-configuration

Explanation

The stereochemistry of the compound is designated as (5S)-configuration according to the IUPAC nomenclature, indicating the spatial arrangement of the atoms around the chiral center.
6. Unique spirocyclic structure

Explanation

The compound features a spirocyclic structure with a seven-membered ring and a six-membered ring, which contributes to its unique properties and potential applications.
7. Presence of a methyl group

Explanation

The compound contains a methyl group (CH3), which is a common functional group in organic chemistry.
8. Presence of a methylene group

Explanation

The compound also contains a methylene group (CH2), which is another common functional group in organic chemistry.
9. Classified as a ketone

Explanation

The compound is classified as a ketone due to the presence of a carbonyl group (C=O) in its structure.
10. Potential applications

Explanation

The compound may have applications in organic synthesis, pharmaceuticals, and materials science due to its unique structural features and potential reactivity.

Upstream product

• 810682-53-2 (S)-3-(Iodomethyl-dimethyl-silanyloxy)-2,2-dimethyl-cyclohexanone 
• 810682-39-4 (S)-3-(Bromomethyl-dimethyl-silanyloxy)-2,2-dimethyl-cyclohexanone 
• 810682-13-4 (1S,5S)-3,3,9,9-Tetramethyl-2-oxa-3-sila-bicyclo[3.3.1]nonan-5-ol 
• 810682-12-3 (S)-3-(Chloromethyl-dimethyl-silanyloxy)-2,2-dimethyl-cyclohexanone 
• 810682-40-7 (5S,7S)-2,2,6,6-Tetramethyl-1,3-dioxa-spiro[4.5]decan-7-ol 
• 954096-32-3 (1S,3S)-1-Hydroxymethyl-2,2-dimethyl-cyclohexane-1,3-diol 
• 87655-21-8 (S)-3-hydroxy-2,2-dimethylcyclohexanone 
• 74-88-4 methyl iodide 
• 810682-14-5 (S)-2,2,6,6-Tetramethyl-1,3-dioxa-spiro[4.5]decan-7-one 

Downstream Products

• 810682-16-7 (S)-8-(4-Methoxy-benzyloxymethyl)-2,2,6,6-tetramethyl-1,3-dioxa-spiro[4.5]dec-7-ene 
• 810682-43-0 (S)-1-Hydroxymethyl-4-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-cyclohex-3-enol 
• 810682-17-8 Acetic acid (S)-1-hydroxy-4-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-cyclohex-3-enylmethyl ester 
• 810682-45-2 [(S)-4-(4-Methoxy-benzyloxymethyl)-1-methoxymethoxy-2,2-dimethyl-cyclohex-3-enyl]-methanol 
• 810682-44-1 Acetic acid (S)-4-(4-methoxy-benzyloxymethyl)-1-methoxymethoxy-2,2-dimethyl-cyclohex-3-enylmethyl ester 
• 810682-15-6 (S)-2,2,6,6-Tetramethyl-8-methylene-1,3-dioxa-spiro[4.5]decan-7-ol 

Relevant academic research and scientific papers

Development of silicon-tethered anionic reaction and its application to the synthesis of chiral A-ring moieties of Taxol

Silicon-tethered intramolecular nucleophilic additions of a hydroxymethyl unit to ketones in β-hydroxyketones have been developed. The product obtained by this protocol was successfully converted to chiral A-ring moieties of Taxol. Also developed was a pr