1426-70-6 Usage
Explanation
These are alternative names for the compound, which are used to describe its structure and properties.
Explanation
A ketone is a type of organic compound that contains a carbonyl group (C=O) bonded to two other carbon atoms. In this case, the carbonyl group is attached to a six-carbon chain and a fluorine-substituted phenyl group.
Explanation
The compound has a linear chain of six carbon atoms, with the first carbon atom bonded to a phenyl group (a six-membered aromatic ring) that has a fluorine atom as a substituent.
Explanation
1-Hexanone, 1-(4-fluorophenyl)is used in the synthesis of various pharmaceuticals and can also act as a solvent in different chemical reactions and processes due to its ability to dissolve a wide range of substances.
Explanation
As with any chemical compound, it is essential to follow proper handling and safety procedures when working with 1-Hexanone, 1-(4-fluorophenyl)to minimize the risk of accidents or exposure to hazardous conditions. This may include wearing personal protective equipment (PPE), working in a well-ventilated area, and following specific guidelines for storage and disposal.
Chemical Class
Ketone
Structure
Six-carbon chain with a fluorine-substituted phenyl group at the first carbon
Applications
Pharmaceutical production, solvent in chemical reactions and processes
Additional Applications
Organic synthesis and research
Safety Measures
Proper handling and precautions required
Check Digit Verification of cas no
The CAS Registry Mumber 1426-70-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1426-70:
(6*1)+(5*4)+(4*2)+(3*6)+(2*7)+(1*0)=66
66 % 10 = 6
So 1426-70-6 is a valid CAS Registry Number.
1426-70-6Relevant articles and documents
Preparation method of aryl ketone compound
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Paragraph 0041-0049; 0061-0065; 0067, (2022/04/16)
The invention provides a preparation method of an aryl ketone compound, and belongs to the technical field of compound synthesis. The method comprises the following steps: under the action of a silver catalyst and water, carrying out reaction on aryl alkyne with a structure as shown in a formula 1 in a solvent at 60-120 DEG C for 12-48 hours, and separating and purifying a product after the reaction is finished, so as to obtain the single aryl ketone compound with a structure as shown in a formula I, the raw materials are easy to obtain, the experimental operation is simple, the yield of the prepared single aryl ketone compound is good, and gram-scale experiments can be carried out.
Acyl hydrazides as acyl donors for the synthesis of diaryl and aryl alkyl ketones
Akhbar, Ahmed R.,Chudasama, Vijay,Fitzmaurice, Richard J.,Powell, Lyn,Caddick, Stephen
, p. 743 - 746 (2014/01/06)
In this communication we describe a novel strategy for the formation of valuable diaryl and aryl alkyl ketones from acyl hydrazides. A wide variety of ketones are prepared and the mild reaction conditions allow for the use of a range of functionalities, especially in the synthesis of diaryl ketones.
Ir- and Ru-catalyzed sequential reactions: Asymmetric α-alkylative reduction of ketones with alcohols
Onodera, Gen,Nishibayashi, Yoshiaki,Uemura, Sakae
, p. 3819 - 3822 (2007/10/03)
(Chemical Equation Presented) The compatibility between [{IrCl(cod)} 2] and ruthenium complex 1 to achieve asymmetric α-alkylative reduction of prochiral ketones with primary alcohols is an essential factor in obtaining optically active alcohols with elongation of the carbon skeleton in good yields with a high enantioselectivity.
