1050169-98-6 Usage
Explanation
Different sources of media describe the Explanation of 1050169-98-6 differently. You can refer to the following data:
1. This is the full IUPAC name of the compound, which describes its structure and stereochemistry.
2. 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
3. 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.
4. The stereochemistry of the compound is described by the (4aS,8aR) configuration, which indicates the spatial arrangement of the atoms in the molecule.
5. The compound may be used in various chemical reactions and processes, and its specific properties and potential applications can be explored in these fields.
6. 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.
7. The compound has a bicyclic structure, with a carbonyl group (C=O) and a phenylmethyl group attached to the naphthalene ring.
8. 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.
9. The reactivity of the compound will depend on the specific reaction conditions, such as temperature, pressure, and the presence of catalysts or other reagents.
10. 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
Check Digit Verification of cas no
The CAS Registry Mumber 1050169-98-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,0,1,6 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1050169-98:
(9*1)+(8*0)+(7*5)+(6*0)+(5*1)+(4*6)+(3*9)+(2*9)+(1*8)=126
126 % 10 = 6
So 1050169-98-6 is a valid CAS Registry Number.
1050169-98-6Relevant 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
Ramachary, Dhevalapally B.,Sakthidevi, Rajasekar
supporting information; experimental part, p. 2488 - 2492 (2009/02/02)
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.
