125996-99-8 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This describes the arrangement of atoms and the type of chemical bonds in the compound.
Explanation
It is classified as an organic compound because it contains carbon and hydrogen atoms.
Explanation
The presence of a trifluoromethyl group (CF3) in the compound provides unique chemical and physical properties.
Explanation
The pent-4-en-1-one functional group is a key structural feature of the compound, which influences its reactivity and properties.
Explanation
It is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique properties.
Explanation
The compound serves as a building block in the production of other organic compounds, contributing to its versatility in chemical synthesis.
Explanation
The trifluoromethyl group imparts unique chemical and physical properties to the compound, making it valuable in synthetic and industrial processes.
Explanation
The compound is used in various applications, including the synthesis of pharmaceuticals, agrochemicals, and other organic compounds, due to its unique properties and reactivity.
Chemical structure
1-[3-(TrifluoroMethyl)phenyl]pent-4-en-1-one
Organic compound
Yes
Contains a trifluoromethyl group
Yes
Contains a pent-4-en-1-one functional group
Yes
Used as an intermediate in synthesis
Yes
Utilized as a building block
Yes
Unique chemical and physical properties
Yes
Applications
Pharmaceutical and agrochemical synthesis, organic compound production
Check Digit Verification of cas no
The CAS Registry Mumber 125996-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,9,9 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 125996-99:
(8*1)+(7*2)+(6*5)+(5*9)+(4*9)+(3*6)+(2*9)+(1*9)=178
178 % 10 = 8
So 125996-99-8 is a valid CAS Registry Number.
125996-99-8Relevant articles and documents
Selective Synthesis of Z-Silyl Enol Ethers via Ni-Catalyzed Remote Functionalization of Ketones
Guven, Sinem,Kundu, Gourab,Rissanen, Kari,Schoenebeck, Franziska,Ward, Jas S.,We?els, Andrea
supporting information, p. 8375 - 8380 (2021/06/27)
We report a remote functionalization strategy, which allows the Z-selective synthesis of silyl enol ethers of (hetero)aromatic and aliphatic ketones via Ni-catalyzed chain walking from a distant olefin site. The positional selectivity is controlled by the directionality of the chain walk and is independent of thermodynamic preferences of the resulting silyl enol ether. Our mechanistic data indicate that a Ni(I) dimer is formed under these conditions, which serves as a catalyst resting state and, upon reaction with an alkyl bromide, is converted to [Ni(II)-H] as an active chain-walking/functionalization catalyst, ultimately generating a stabilized η3-bound Ni(II) enolate as the key selectivity-controlling intermediate.