115356-18-8 Usage
Explanation
This is the IUPAC name of the compound, which describes its structure and stereochemistry.
Explanation
The molecular formula represents the number of carbon (C), hydrogen (H), and oxygen (O) atoms in the compound, which is 15, 22, and 2, respectively.
Explanation
The compound is classified as a ketone due to the presence of a carbonyl group (C=O) in its structure.
Explanation
The compound has a tetrahydro-4-(1-hydroxy-1-methylethyl) group, which is a saturated hydrocarbon with a hydroxyl (OH) and a methyl (CH3) group, attached to the specified carbon atoms of the naphthalene ring.
Explanation
The compound has two additional methyl groups attached to the 4a and 5 carbon atoms of the naphthalene ring.
Explanation
The stereochemistry of the compound is described by the (4R,4aR,5R) configuration, which indicates the spatial arrangement of the atoms at the 4th, 4a, and 5th carbon atoms.
Explanation
The compound may have different applications in fields such as chemistry, pharmaceuticals, or materials science, but further research is needed to determine its specific uses.
Explanation
As with any chemical compound, it is important to handle and use 1(4H)-Naphthalenone,4a,5,6,7-tetrahydro-4-(1-hydroxy-1-methylethyl)-4a,5-dimethyl-, (4R,4aR,5R)- carefully to avoid potential hazards or adverse effects. This includes following safety protocols and guidelines to minimize risks.
Classification
Ketone
Structure
Tetrahydro-4-(1-hydroxy-1-methylethyl) group attached to the 4th, 5th, 6th, and 7th carbon atoms of the naphthalene ring
Methyl Groups
Two methyl groups at the 4a and 5 carbon atoms
Stereochemistry
(4R,4aR,5R)
Applications
Various potential applications
Safety
Handle and use with caution, following proper safety protocols and guidelines
Check Digit Verification of cas no
The CAS Registry Mumber 115356-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,5 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 115356-18:
(8*1)+(7*1)+(6*5)+(5*3)+(4*5)+(3*6)+(2*1)+(1*8)=108
108 % 10 = 8
So 115356-18-8 is a valid CAS Registry Number.
115356-18-8Relevant academic research and scientific papers
Extracyclic Stereocontrolled Alkylation of (1R,5S)-4-Ethyl-6,6-dimethyl-3-(phenylsulfonyl)bicyclohept-3-en-2-one. A Highly Stereocontrolled Synthesis of (-)-Kanshone A
Kato, Michiharu,Watanabe, Masataka,Awen, Bahlul, Z.
, p. 5145 - 5152 (2007/10/02)
(1R,5S)-4-Ethyl-6,6-dimethyl-3-(phenylsulfonyl)bicyclohept-3-en-2-one (7) was prepared from (+)-nopinone (1) in six steps and 70percent overall yield via (1R,5R)-6,6-dimethyl-3-(phenylthio)bicyclohept-3-en-2-one (2).Alkylation reactions of 7
Total Synthesis of Kanshone A, a Sesquiterpene Isolated from Nardostachys chinensis (Valerianaceae)
Tori, Motoo,Furuta, Hirosuke,Asakawa, Yoshinori
, p. 1919 - 1922 (2007/10/02)
Kanshone A, isolated from Nardostachys chinensis (Valerianaceae), has been synthesized in 9 steps by stereoselective alkylation of the derivative methyl (5,5-ethylenedioxy-1,2-dimethylcyclohexyl)acetate and an intramolecular aldol cyclization followed by methylation and introduction of a double bond
A highly stereocontrolled synthesis of (-)-kanshone A
Kato,Watanabe,Awen
, p. 7443 - 7444 (2007/10/02)
Described herein is the first and stereoselective synthesis of (-)-kanshone A (3), a nardosinan sesquiterpene, starting with enone 2.
