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1-Phenyl-5-cyclohexyl-3-pentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54986-38-8

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54986-38-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54986-38-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,9,8 and 6 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54986-38:
(7*5)+(6*4)+(5*9)+(4*8)+(3*6)+(2*3)+(1*8)=168
168 % 10 = 8
So 54986-38-8 is a valid CAS Registry Number.

54986-38-8Downstream Products

54986-38-8Relevant academic research and scientific papers

C-H and C-C bond activation of primary amines through dehydrogenation and transimination

Jun, Chul-Ho,Chung, Kwan-Yong,Hong, Jun-Bae

, p. 785 - 787 (2007/10/03)

Matrix presented Dehydrogenation and subsequent transimination of primary amines offer a new pathway for C-H bond activation, ortho-alkylation, and C-C bond activation to afford a variety of ketones in the reaction of 1-alkene by a cocatalyt system of Rh(I) and 2-amino-3-picoline.

Catalytic activation of C-H and C-C bonds of allylamines via olefin isomerization by transition metal complexes

Jun, Chul-Ho,Lee, Hyuk,Park, Jae-Bum,Lee, Dae-Yon

, p. 2161 - 2164 (2008/02/11)

(matrix presented) The metal-catalyzed reaction of olefins with allylamines bearing coordination sites (2-pyridyl groups) was studied. With Ru3(CO)12 as catalyst, activation of C-H bonds led to the formation of ketimines that were hydrolyzed to give asymmetric ketones. With [(C8H14)2RhCl]2, both C-H and C-C bonds were activated and symmetric ketones were formed on hydrolysis. The reaction involves double bond migration of the allylamine to form an aldimine.

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