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2-Propen-1-one, 1-(2-hydroxyphenyl)-3-(4-pyridinyl)-, also known as 1-(2-hydroxyphenyl)-3-(4-pyridinyl)-2-propen-1-one, is a chemical compound with the molecular formula C15H11NO2. It is a derivative of 2-propen-1-one, featuring a 2-hydroxyphenyl group attached to the 1-position and a 4-pyridinyl group at the 3-position. 2-Propen-1-one, 1-(2-hydroxyphenyl)-3-(4-pyridinyl)- is characterized by its conjugated system, which includes the carbonyl group, the phenyl ring, and the pyridine ring, providing it with unique electronic properties. It is an organic molecule that can be found in various chemical and pharmaceutical applications, such as in the synthesis of certain drugs and other organic compounds. The compound's structure and properties make it a subject of interest in organic chemistry, particularly in the study of conjugated systems and their effects on reactivity and stability.

2875-27-6

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2875-27-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2875-27-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2875-27:
(6*2)+(5*8)+(4*7)+(3*5)+(2*2)+(1*7)=106
106 % 10 = 6
So 2875-27-6 is a valid CAS Registry Number.

2875-27-6SDS

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-(2-hydroxyphenyl)-3-pyridin-4-ylprop-2-en-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

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More Details:2875-27-6 SDS

2875-27-6Relevant academic research and scientific papers

Convenient synthesis of flavanone derivatives via oxa-Michael addition using catalytic amount of aqueous cesium fluoride

Miura, Motofumi,Shigematsu, Karin,Toriyama, Masaharu,Motohashi, Shigeyasu

supporting information, (2021/10/25)

A total of 36 flavanones, which included polycyclic aromatic and heterocyclic rings, were readily synthesized via oxa-Michael addition from the corresponding hydroxychalcones with a catalytic amount of aqueous cesium fluoride solution under mild conditions. This method could be applied to the scalable synthesis of eriodictyol as a known potent inhibitor of the SARS-CoV-2 spike protein.

Photochemical behavior of 2'-hydroxychalcone derivatives having pyridyl and quinolyl groups

Aizawa, Fumiya,Shinozaki, Yukino,Ishida, Yuka,Arai, Tatsuo

, p. 572 - 579 (2017/04/10)

2'-Hydroxy chalcone derivatives having heteroaromatic rings have been synthesized and their photochemical and photophysical properties have been examined in terms of tautomer produced by intramolecular hydrogen atom transfer reaction.

Inhibitory Kinetics of Azachalcones and their Oximes on Mushroom Tyrosinase: A Facile Solid-state Synthesis

Radhakrishnan, Sini K.,Shimmon, Ronald G.,Conn, Costa,Baker, Anthony T.

, p. 531 - 538 (2016/06/01)

A solid-state-based mechanochemical process was used to synthesize novel azachalcones and their oximes as tyrosinase inhibitors. Their inhibitory activities on mushroom tyrosinase using l-3,4-dihydroxyphenylalanine as a substrate were investigated. Two of

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