10323-98-5 Usage
Description
5-(3-nitrophenyl)-3-methylcyclohex-2-enone is an organic compound derived from acetone, a common organic building block in organic chemistry. It features a cyclohexenone ring with a methyl group at the 3-position and a nitrophenyl group at the 5-position. 5-(3-nitrophenyl)-3-methylcyclohex-2-enone has potential applications in various industries due to its unique chemical structure and properties.
Uses
Used in Chemical Synthesis:
5-(3-nitrophenyl)-3-methylcyclohex-2-enone is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows for further functionalization and modification, making it a versatile building block for creating complex molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-(3-nitrophenyl)-3-methylcyclohex-2-enone is used as a key intermediate for the development of novel drugs. Its chemical properties enable it to be incorporated into drug molecules targeting specific biological pathways, potentially leading to the discovery of new therapeutic agents.
Used in Flavor and Fragrance Industry:
5-(3-nitrophenyl)-3-methylcyclohex-2-enone may also find applications in the flavor and fragrance industry due to its potential to contribute unique scents or flavors when used as a component in the creation of various compounds.
Used in Material Science:
The compound's structural features may also make it suitable for use in material science, where it could be employed in the development of new materials with specific properties, such as improved stability or reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 10323-98-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,2 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10323-98:
(7*1)+(6*0)+(5*3)+(4*2)+(3*3)+(2*9)+(1*8)=65
65 % 10 = 5
So 10323-98-5 is a valid CAS Registry Number.
10323-98-5Relevant articles and documents
D-Aminoacylase-initiated cascade Aldol condensation/Robinson annulation for synthesis of substituted cyclohex-2-enones from simple aldehydes and acetone
Xiang, Ziwei,Liang, Yiru,Chen, Xiang,Wu, Qi,Lin, Xianfu
, p. 1929 - 1937 (2014/08/05)
As an important building block, developing efficient and green synthesis strategy of cyclohex-2-enones is of great importance. In this present work, a general approach to the mild synthesis of substituted cyclohex-2-enones derivatives starting fro m simple aldehydes and acetone have been achieved via D-aminoacylase-initiated Aldol condensation/Robinson annulation cascade reaction using imidazole as an additive in organic media. The influences of reaction conditions including solvents, enzyme concentration, additives type, molar ratio of enzyme to additive, and substrate scopes were systematically investigated. Furthermore, some experiments were designed to explore the catalytic roles of D-aminoacylase and imidazole in the multistep cascade process, and one possible mechanism was proposed.
