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(±)-1,5-diphenyl-2,4-dipropylpentane-1,5-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1609404-80-9

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1609404-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1609404-80-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,4,0 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1609404-80:
(9*1)+(8*6)+(7*0)+(6*9)+(5*4)+(4*0)+(3*4)+(2*8)+(1*0)=159
159 % 10 = 9
So 1609404-80-9 is a valid CAS Registry Number.

1609404-80-9Downstream Products

1609404-80-9Relevant academic research and scientific papers

Rhodium-catalyzed ketone methylation using methanol under mild conditions: Formation of α-branched products

Chan, Louis K. M.,Poole, Darren L.,Shen, Di,Healy, Mark P.,Donohoe, Timothy J.

, p. 761 - 765 (2014)

The rhodium-catalyzed methylation of ketones has been accomplished using methanol as the methylating agent and the hydrogen-borrowing method. The sequence is notable for the relatively low temperatures that are required and for the ability of the reaction system to form α-branched products with ease. Doubly alkylated ketones can be prepared from methyl ketones and two different alcohols by using a sequential one-pot iridium- and rhodium-catalyzed process. Uniquely effective for making branched alkyl products from ketones (see scheme): The scope of the presented reaction includes aromatic and aliphatic ketones and consecutive one-pot double alkylation reactions to provide a convenient route to branched ketones from simple methyl ketones. A brief study into the mechanism of the reaction has given evidence for an aldol-based reaction pathway.

Cobalt(II)porphyrin-Mediated Selective Synthesis of 1,5-Diketones via an Interrupted-Borrowing Hydrogen Strategy Using Methanol as a C1 Source

Biswal, Priyabrata,Samser, Shaikh,Nayak, Prakash,Chandrasekhar, Vadapalli,Venkatasubbaiah, Krishnan

, p. 6744 - 6754 (2021/05/29)

A novel cobalt(II)porphyrin-mediated acceptorless dehydrogenation of methanol is reported for the first time. This methodology has been applied for the coupling of a variety of ketones with methanol to produce 1,5-diketones along with H2 and H2O as the environment friendly byproducts. This paradigm was also demonstrated for a one-pot synthesis of substituted pyridines using a sequential addition protocol where the 1,5-diketones were generated in situ. From many experiments including those involving deuterium labeling, it is proposed that protonated cobalt(II)porphyrin methoxide complex acts as an intermediate to generate formaldehyde along with a metal hydride.

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