174485-37-1 Usage
Description
1-(4-Fluoro-phenyl)-hexan-3-one, a chemical compound with the molecular formula C12H15FO, is a ketone characterized by a six-carbon chain with a fluorine-substituted phenyl group attached at the first carbon and a carbonyl group at the third carbon. It is used in the synthesis of various pharmaceuticals and organic compounds and can also serve as a building block for the production of other chemicals.
Uses
Used in Pharmaceutical Industry:
1-(4-Fluoro-phenyl)-hexan-3-one is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties.
Used in Agrochemicals:
In the agrochemical industry, 1-(4-Fluoro-phenyl)-hexan-3-one is used as a precursor in the production of certain agrochemicals, contributing to the development of effective pest control agents.
Used in Cosmetic Industry:
1-(4-Fluoro-phenyl)-hexan-3-one is used as a fragrance ingredient in the cosmetic industry, providing unique scents and enhancing the sensory experience of cosmetic products.
Safety and Handling:
1-(4-Fluoro-phenyl)-hexan-3-one should be handled with care, and its use should be in accordance with proper safety protocols and regulations to ensure the safety of workers and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 174485-37-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,4,8 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 174485-37:
(8*1)+(7*7)+(6*4)+(5*4)+(4*8)+(3*5)+(2*3)+(1*7)=161
161 % 10 = 1
So 174485-37-1 is a valid CAS Registry Number.
174485-37-1Relevant articles and documents
Heck reactions of aryl bromides with alk-1-en-3-ol derivatives catalysed by a tetraphosphine/palladium complex
Berthiol, Florian,Doucet, Henri,Santelli, Maurice
, p. 5633 - 5636 (2007/10/03)
cis,cis,cis-1,2,3,4-Tetrakis(diphenylphosphinomethyl)cyclopentane/ [PdCl(C3H5)]2 efficiently catalyses the Heck reaction of alk-1-en-3-ol with a variety of aryl bromides. In the presence of hex-1-en-3-ol or oct-1-en-3-ol, the β-arylated carbonyl compounds were selectively obtained. Linalool and 2-methylbut-3-en-2-ol led to the corresponding 1-arylalk-1-en-3-ol derivatives. Turnover numbers up to 69,000 can be obtained for this reaction. A minor electronic effect of the substituents of the aryl bromide was observed. Similar reaction rates were observed in the presence of activated aryl bromides such as bromoacetophenone and deactivated aryl bromides such as bromoanisole.
