1050169-98-6

Basic information

• Product Name: 1,6(2H,5H)-Naphthalenedione, hexahydro-8a-(phenylMethyl)-, (4aS,8aR)-
• Synonyms: 1,6(2H,5H)-Naphthalenedione, hexahydro-8a-(phenylMethyl)-, (4aS,8aR)-;(4AS,8AR)-8A-BENZYLHEXAHYDRONAPHTHALENE-1,6(2H,7H)-DIONE
• CAS NO: 1050169-98-6
• Molecular Formula: C₁₇H₂₀O₂
• Molecular Weight: 256.3395
• EINECS: -0
• Mol File: 1050169-98-6.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,6(2H,5H)-Naphthalenedione, hexahydro-8a-(phenylMethyl)-, (4aS,8aR)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6(2H,5H)-Naphthalenedione, hexahydro-8a-(phenylMethyl)-, (4aS,8aR)-(1050169-98-6)
• EPA Substance Registry System: 1,6(2H,5H)-Naphthalenedione, hexahydro-8a-(phenylMethyl)-, (4aS,8aR)-(1050169-98-6)

Safety Data

• Hazardous Substances Data: 1050169-98-6(Hazardous Substances Data)

Usage

Explanation

This is the full IUPAC name of the compound, which describes its structure and stereochemistry.

Explanation

The compound belongs to the class of naphthalenedione, which are organic compounds derived from naphthalene with a carbonyl group (C=O) in the 1,4or 2,3-positions.
3. Hexahydro-8a-(phenylMethyl) group

Explanation

The compound contains a hexahydro (six hydrogen atoms) group attached to the 8a position of the naphthalene ring, and a phenylmethyl (benzene ring with a methyl group) group.

Explanation

The stereochemistry of the compound is described by the (4aS,8aR) configuration, which indicates the spatial arrangement of the atoms in the molecule.

Explanation

The compound may be used in various chemical reactions and processes, and its specific properties and potential applications can be explored in these fields.

Explanation

More research and testing may be required to fully understand the characteristics and uses of this compound, as its properties and applications are not yet fully known.

Explanation

The compound has a bicyclic structure, with a carbonyl group (C=O) and a phenylmethyl group attached to the naphthalene ring.

Explanation

The compound contains functional groups such as a carbonyl group, a phenyl group, and a methyl group, which contribute to its chemical properties and reactivity.

Explanation

The reactivity of the compound will depend on the specific reaction conditions, such as temperature, pressure, and the presence of catalysts or other reagents.

Explanation

The solubility of the compound in various solvents is not known without conducting solubility experiments.

Type

Naphthalenedione

Stereochemistry

(4aS,8aR)

Potential Applications

Organic Chemistry, Pharmaceuticals, Materials Science

Further Research

Necessary

Structure

Bicyclic with a carbonyl group and a phenylmethyl group

Functional Groups

Carbonyl, Phenyl, Methyl

Reactivity

Depends on the specific reaction conditions and reagents

Solubility

Unknown without experimental data

Upstream product

• 154471-45-1 8a-Benzyl-3,4,8,8a-tetrahydro-2H,7H-naphthalene-1,6-dione 

Relevant articles and documents

Combining multi-catalysis and multi-component systems for the development of one-pot asymmetric reactions: Stereoselective synthesis of highly functionalized bicyclo[4.4.0]decane-1,6-diones

We have developed a direct amine/acid-catalyzed stereoselective hydrogenation of a variety of Wieland-Miescher (W-M) ketones, Hajos-Parrish (H-P) ketones and their analogs with organic hydrides (Hantzsch esters) as the hydrogen source. This astonishingly simple and biomimetic approach was used to construct highly functionalized chiral bicyclo[4.4.0]decane-1,6-diones 6 in a diastereoselective fashion. This is an example of the development of a new technology by the combination of multiple catalysts and components in one pot to deliver highly functionalized chiral molecules. The Royal Society of Chemistry 2008.