34311-15-4 Usage
Explanation
The IUPAC name is a standardized nomenclature system used to name chemical compounds. It provides information about the structure and stereochemistry of the molecule.
Explanation
The common name is a more familiar and easily recognizable name for the compound, often used in everyday language and industry.
Explanation
1(2H)-Naphthalenone, 3,4-dihydro-2-methyl-, (2S)- is naturally present in the essential oils of certain plants, which can be extracted and used in various applications.
Explanation
The compound has a characteristic minty and fresh scent, which makes it desirable for use in the fragrance and flavor industries.
Explanation
Due to its pleasant aroma and potential health benefits, 1(2H)-Naphthalenone, 3,4-dihydro-2-methyl-, (2S)- is used in various industries, including the production of perfumes, soaps, and other scented products, as well as in the development of pharmaceuticals.
Explanation
The (2S)notation indicates the stereochemistry of the molecule, specifically the configuration of the chiral center at the 2nd carbon atom. This can affect the compound's properties and biological activity.
Explanation
The (-) sign in the common name indicates that the compound is optically active and exhibits a negative rotation of plane-polarized light, which is a property of chiral compounds.
Explanation
As an organic compound, it is expected to be soluble in nonpolar or slightly polar organic solvents such as ethanol, acetone, or diethyl ether.
Explanation
The compound is generally stable when stored and handled properly, avoiding extreme temperatures, light, or moisture.
Natural Occurrence
Found in essential oils such as caraway and spearmint
Aroma
Minty, fresh
Applications
Fragrance and flavor industries, pharmaceuticals (antimicrobial and anti-inflammatory properties)
Chirality
(2S)-
Optical Activity
(-) Sign
Solubility
Generally soluble in organic solvents
Stability
Stable under normal conditions
Check Digit Verification of cas no
The CAS Registry Mumber 34311-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,3,1 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 34311-15:
(7*3)+(6*4)+(5*3)+(4*1)+(3*1)+(2*1)+(1*5)=74
74 % 10 = 4
So 34311-15-4 is a valid CAS Registry Number.
34311-15-4Relevant academic research and scientific papers
Organocatalytic enantioselective protonation of silyl enolates mediated by cinchona alkaloids and a latent source of HF
Poisson, Thomas,Dalla, Vincent,Marsais, Francis,Dupas, Georges,Oudeyer, Sylvain,Levacher, Vincent
, p. 7090 - 7093 (2008/09/17)
Hidden benefits: The enantioselective organocatalytic protonation of silyl enolates has been achieved by using readily available cinchona alkaloid catalysts (1) and a latent source of HF that delivers "at will" the active catalytic hydrogen fluoride salt
Catalytic enantioselective decarboxylative protonation
Mohr, Justin T.,Nishimata, Toyoki,Behenna, Douglas C.,Stoltz, Brian M.
, p. 11348 - 11349 (2007/10/03)
We report a highly enantioselective, general catalytic system for the facile synthesis of tertiary stereocenters by protonation adjacent to cyclic ketones. The method relies on catalytic decarboxylative protonation of readily accessible racemic quaternary β-ketoesters. A range of substituted cycloalkanone compounds can be accessed through this process with high levels of enantioselectivity. Copyright
