90105-53-6 Usage
Type of compound
Cyclic diketone
It is a type of organic compound that contains a cyclic structure with two carbonyl (C=O) groups.
Usage
Building block in organic synthesis
It serves as an intermediate or starting material for the synthesis of various other compounds.
Applications
Pharmaceutical, agrochemical, and flavoring agent
It is used in the production of pharmaceuticals, agrochemicals, and as a flavoring agent in the food industry.
Physical state
Clear, colorless liquid
The compound appears as a transparent, colorless liquid at room temperature.
Odor
Slightly sweet
It has a mild, sweet smell.
Solubility
Soluble in water and most organic solvents
The compound can dissolve in water and is also soluble in various organic solvents, making it versatile for different chemical reactions.
Industrial importance
Valuable intermediate
It is considered a valuable intermediate in the synthesis of various compounds, contributing to its range of industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 90105-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,0 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90105-53:
(7*9)+(6*0)+(5*1)+(4*0)+(3*5)+(2*5)+(1*3)=96
96 % 10 = 6
So 90105-53-6 is a valid CAS Registry Number.
90105-53-6Relevant academic research and scientific papers
A Scalable Protocol for the Regioselective Alkylation of 2-Methylcyclohexane-1,3-dione with Unactivated sp3 Electrophiles
Sharpe, Robert J.,Portillo, Maribel,Vélez, Robert A.,Johnson, Jeffrey S.
supporting information, p. 2293 - 2295 (2015/09/28)
A method for the C-selective alkylation of 2-methylcyclohexane-1,3-dione with unactivated sp3 electrophiles is accomplished via alkylation and subsequent deprotection of the derived ketodimethyl hydrazones. The present method provides a high-yielding entry to dialkyl cycloalkanones that cannot be accessed via direct alkylation of 2-methylcyclohexane-1,3-dione. The title reaction may be useful in the scalable preparation of terpene and steroidal building blocks in the arena of natural product synthesis.
CHIRAL CYCLOHEXANOID SYNTHETIC PRECURSORS VIA ASYMMETRIC MICROBIAL REDUCTION OF PROCHIRAL CYCLOHEXANEDIONES
Brooks, Dee W.,Mazdiyasni, Hormoz,Chakrabarti, Sharmistha
, p. 1241 - 1244 (2007/10/02)
Microbial reduction of various 2,2-disubstituted-1,3-cyclohexanediones with bakers' yeast provides efficient access to chiral cyclohexanoid synthetic precursors.
