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4-((dimethylamino)phenyl)(1-hydroxycyclohexyl)methanone is a complex organic compound with the molecular formula C17H23NO2. It features a dimethylamino group attached to a phenyl ring, which is connected to a cyclohexane ring through a methylene bridge. The cyclohexane ring has a hydroxyl group at the 1-position, and the entire structure is characterized by its amine and ketone functional groups. 4-((dimethylamino)phenyl)(1-hydroxycyclohexyl)methanone is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, particularly those with biological activity. Its specific properties and reactivity make it a valuable intermediate in organic synthesis, though it is important to handle such chemicals with care due to their potential toxicity and reactivity.

4842-66-4

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4842-66-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4842-66-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,4 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4842-66:
(6*4)+(5*8)+(4*4)+(3*2)+(2*6)+(1*6)=104
104 % 10 = 4
So 4842-66-4 is a valid CAS Registry Number.

4842-66-4Upstream product

4842-66-4Downstream Products

4842-66-4Relevant academic research and scientific papers

Magnesium Aldimines Prepared by Addition of Organomagnesium Halides to 2,4,6-Trichlorophenyl Isocyanide: Synthesis of 1,2-Dicarbonyl Derivatives

Schw?rzer, Kuno,Bellan, Andreas,Z?schg, Maximilian,Karaghiosoff, Konstantin,Knochel, Paul

, p. 9415 - 9418 (2019)

The selective addition of organomagnesium reagents to 2,4,6-trichlorophenyl isocyanide leading to magnesiated aldimines is reported. These aldimines react with Weinreb amides, ketones, or carbonates to provide the corresponding carbonyl derivatives after acidic cleavage. This allows for an efficient synthesis of 1,2-dicarbonyl compounds and α-hydroxy ketones.

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