174485-37-1 Usage
General Description
1-(4-Fluoro-phenyl)-hexan-3-one is a chemical compound with the molecular formula C12H15FO. It 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. 1-(4-FLUORO-PHENYL)-HEXAN-3-ONE is used in the synthesis of various pharmaceuticals and organic compounds, and it can also be used as a building block for the production of other chemicals. It has potential applications in the pharmaceutical industry, agrochemicals, and as a fragrance ingredient in the cosmetic industry. 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.
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.
