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125996-99-8

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125996-99-8 Usage

Explanation

Different sources of media describe the Explanation of 125996-99-8 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule of the compound.
2. This describes the arrangement of atoms and the type of chemical bonds in the compound.
3. It is classified as an organic compound because it contains carbon and hydrogen atoms.
4. The presence of a trifluoromethyl group (CF3) in the compound provides unique chemical and physical properties.
5. The pent-4-en-1-one functional group is a key structural feature of the compound, which influences its reactivity and properties.
6. It is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique properties.
7. The compound serves as a building block in the production of other organic compounds, contributing to its versatility in chemical synthesis.
8. The trifluoromethyl group imparts unique chemical and physical properties to the compound, making it valuable in synthetic and industrial processes.
9. 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.

125996-99-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[3-(trifluoromethyl)phenyl]pent-4-en-1-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:125996-99-8 SDS

125996-99-8Downstream Products

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.

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