887574-84-7 Usage
Chemical Structure
1-[4-(4-propyl-phenoxy)-phenyl]-ethanone
Explanation
This structure describes the arrangement of atoms and the type of chemical bonds between them. It is a ketone derivative with a phenyl ring substituted with a propyl group and a phenoxy group.
Explanation
These are the specific functional groups present in the compound. The propyl group is a three-carbon alkyl chain (-CH2CH2CH3), and the phenoxy group is a phenol derivative with an oxygen atom bonded to a phenyl ring.
Explanation
This compound is used as an intermediate in the synthesis of various organic compounds and serves as a building block for the production of other chemicals, making it valuable in the chemical industry.
Explanation
Due to its potential hazards, it is important to follow proper safety protocols and handle this compound with care to avoid accidents or health risks.
Explanation
While the exact physical state is not provided, most organic compounds with a molecular weight similar to this one are solids or liquids at room temperature.
Explanation
Compounds with a significant nonpolar character, like this one, are generally soluble in nonpolar organic solvents such as hexane, toluene, or dichloromethane.
Explanation
The compound is likely stable under normal conditions, such as room temperature and pressure, and in the absence of strong acids, bases, or oxidizing agents.
Explanation
The compound may undergo chemical reactions when exposed to strong acids, bases, or oxidizing agents, which can alter its structure and properties.
Type of Compound
Ketone derivative
Functional Groups
Propyl group, Phenoxy group
Application
Organic synthesis and building block for other chemicals
Hazardous Nature
Handle with caution
Physical State
Likely a solid or liquid at room temperature
Solubility
Soluble in organic solvents
Stability
Stable under normal conditions
Reactivity
Reactive with strong acids, bases, and oxidizing agents
Check Digit Verification of cas no
The CAS Registry Mumber 887574-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,5,7 and 4 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 887574-84:
(8*8)+(7*8)+(6*7)+(5*5)+(4*7)+(3*4)+(2*8)+(1*4)=247
247 % 10 = 7
So 887574-84-7 is a valid CAS Registry Number.
887574-84-7Relevant articles and documents
Nickel-Catalyzed Etherification of Phenols and Aryl Halides through Visible-Light-Induced Energy Transfer
Zhu, Da-Liang,Jiang, Shan,Wu, Qi,Wang, Hao,Li, Hai-Yan,Li, Hong-Xi
supporting information, p. 8327 - 8332 (2021/10/25)
Notwithstanding some progress in nickel-catalyzed etherification of alkanols and arylhalides, the ability of such a Ni-catalyzed transformation employing phenols to diaryl ethers is unsuccessful due to phenolates with much lower reduction potentials, which suppress the oxidation of nickel(II) intermediates into requisite Ni(III) species. We herein report visible-light-initiated, nickel-catalyzed O-arylation of phenols with arylhalides using t-BuNH(i-Pr) as the base and thioxanthen-9-one as the photosensitizer under visible light. This photocoupling exhibits a broad substrate scope.
