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1-Phenyl-4-(pyridin-2-yl)butan-1-one is an organic compound with the molecular formula C15H15NO. It is a derivative of butanone, featuring a phenyl group (C6H5) at the 1st position and a pyridin-2-yl group (C5H4N) at the 4th position. This molecule is characterized by its unique structure, which combines the aromatic properties of the phenyl and pyridinyl groups with the aliphatic nature of the butanone backbone. The compound may exhibit various chemical and physical properties, such as solubility in organic solvents and potential reactivity with nucleophiles or electrophiles, due to the presence of these functional groups. Its synthesis and applications may involve the use of 1-phenyl-4-(pyridin-2-yl)butan-1-one as an intermediate in the preparation of more complex molecules or as a building block in medicinal chemistry and material science.

7153-77-7

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7153-77-7 Usage

Class

1-Phenyl-4-(pyridin-2-yl)butan-1-one belongs to the class of ketones.

Molecular weight

223.27 g/mol

Chemical structure

A phenyl group is attached to a butanone chain, with a pyridin-2-yl substituent at the fourth carbon atom.

Uses

It is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds, particularly in the development of drugs targeting neurological disorders and behavior regulation. It is also utilized in research and development within the chemical and pharmaceutical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 7153-77-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,5 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7153-77:
(6*7)+(5*1)+(4*5)+(3*3)+(2*7)+(1*7)=97
97 % 10 = 7
So 7153-77-7 is a valid CAS Registry Number.

7153-77-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-4-pyridin-2-ylbutan-1-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:7153-77-7 SDS

7153-77-7Relevant academic research and scientific papers

Silver-Promoted Radical Ring-Opening/Pyridylation of Cyclobutanols with N-Methoxypyridinium Salts

Chen, Yu,Zhang, Guang-Yi,Guo, Chan,Lan, Ping,Banwell, Martin G.,He, Yu-Tao

, (2022/03/03)

The silver-promoted reaction of tertiary cyclobutanols with N-methoxypyridinium salts enables the efficient synthesis of a range of C2-substituted pyridines. The overall process likely occurs by ring-opening (via β-scission) of the cyclobutoxy radical to generate the corresponding γ-keto alkyl radical that itself adds to the pyridinium salt. A wide range of tertiary cyclobutanols and N-methoxypyridinium salts are compatible with the reaction conditions.

4-substituted octahydroquinolizine analgesic compounds and octahydroquinolizinium intermediates

-

, (2008/06/13)

Octahydroquinolizine and corresponding octahydroquinolizinium compounds of formulae (I) and (Va): STR1 where A is a 3 to 7 membered carbocyclic ring, R1 is a substituent, n is 0-2, x is 0-3, and Y is an anion. Also, pharmaceutical compositions

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