810682-18-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 14 carbon (C) atoms, 24 hydrogen (H) atoms, and 2 oxygen (O) atoms.
Explanation
Cyclohexanones are a class of organic compounds that contain a cyclohexane ring with a keto group (C=O) substitution. 1,3-Dioxaspiro[4.5]decan-7-one,2,2,6,6,8-pentamethyl-,(5S)-(9CI) belongs to this class.
Explanation
The compound is a liquid at room temperature, and it is colorless and flammable, which means it can easily catch fire when exposed to a source of ignition.
Explanation
The compound has a pleasant, flower-like scent, making it suitable for use in the fragrance and flavor industry.
Explanation
Due to its floral odor and potential medicinal properties, the compound is used in various industries, including the creation of fragrances, flavors, and pharmaceutical drugs, as well as in the production of personal care and household products.
Explanation
The compound has potential applications in the development of pharmaceutical drugs, as it can be used as a building block or intermediate in the synthesis process.
Explanation
As with any chemical compound, it is essential to handle this substance with care and follow safety guidelines to minimize health risks and ensure safe usage.
Explanation
The compound has a chiral center at the 5th carbon atom, and the (5S)-configuration indicates that the hydroxyl group (-OH) is on the same side as the hydrogen atom when viewed from the backside of the molecule.
Class
Cyclohexanones
Physical State
Colorless, flammable liquid
Odor
Floral
Applications
Fragrance and flavor industry, pharmaceutical synthesis, perfumes, soaps, and other consumer products
Potential Medicinal Properties
Used in the synthesis of various pharmaceutical drugs
Safety Precautions
Handle with care, follow proper safety guidelines
Chirality
(5S)-configuration
Check Digit Verification of cas no
The CAS Registry Mumber 810682-18-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,0,6,8 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 810682-18:
(8*8)+(7*1)+(6*0)+(5*6)+(4*8)+(3*2)+(2*1)+(1*8)=149
149 % 10 = 9
So 810682-18-9 is a valid CAS Registry Number.
810682-18-9Relevant articles and documents
Formal total synthesis of (-)-taxol through Pd-catalyzed eight-membered carbocyclic ring formation
Hirai, Sho,Utsugi, Masayuki,Iwamoto, Mitsuhiro,Nakada, Masahisa
, p. 355 - 359 (2015/02/19)
A formal total synthesis of (-)-taxol by a convergent approach utilizing Pd-catalyzed intramolecular alkenylation is described. Formation of the eight-membered carbocyclic ring has been a problem in the convergent total synthesis of taxol but it was solved by the Pd-catalyzed intramolecular alkenylation of a methyl ketone affording the cyclized product in excellent yield (97 %), indicating the high efficiency of the Pd-catalyzed intramolecular alkenylation. Rearrangement of the epoxy benzyl ether through a 1,5-hydride shift, generating the C3 stereogenic center and subsequently forming the C1-C2 benzylidene, was discovered and utilized in the preparation of a substrate for the Pd-catalyzed reaction.
Construction of the taxane skeleton via the stereoselective conjugate addition of cyanide and the intramolecular B-alkyl Suzuki-Miyaura coupling reaction
Utsugi, Masayuki,Kamada, Yasuaki,Miyamoto, Hidetoshi,Nakada, Masahisa
, p. 6868 - 6872 (2008/02/12)
Construction of the taxane skeleton via the stereoselective conjugate addition of cyanide and the intramolecular B-alkyl Suzuki-Miyaura coupling reaction is described. A conjugate addition of cyanide to enone 17 proceeded diastereoselectively to provide t
Development of silicon-tethered anionic reaction and its application to the synthesis of chiral A-ring moieties of Taxol
Iwamoto, Mitsuhiro,Miyano, Masayuki,Utsugi, Masayuki,Kawada, Hatsuo,Nakada, Masahisa
, p. 8647 - 8651 (2007/10/03)
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
