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1-[2-(4-CHLOROPHENYL)-2-OXOETHYL]-2(1H)-PYRIDINONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108664-55-7

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108664-55-7 Usage

Chemical structure

The compound consists of a pyridinone ring with a 4-chlorophenyl group and an oxoethyl substituent.

Pharmaceutical research

It is commonly used in pharmaceutical research and drug development due to its potential medicinal properties.

Applications

The compound may have applications in the treatment of various diseases and disorders, such as cancer, inflammation, and neurological conditions.

Chemical properties

Its chemical structure and properties make it a valuable target for further investigation and potential therapeutic use.

Molecular weight

The molecular weight of the compound is approximately 271.7 g/mol.

Appearance

The compound is likely to be a solid, based on its molecular weight and structure.

Solubility

The compound may be soluble in organic solvents such as dimethyl sulfoxide (DMSO) or methanol, but its exact solubility profile is not provided in the material.

Stability

The stability of the compound under various conditions (e.g., temperature, pH, light exposure) is not provided in the material.

Synthesis

The synthesis of the compound is not described in the material, but it likely involves the formation of the pyridinone ring and subsequent functionalization with the 4-chlorophenyl and oxoethyl groups.

Biological activity

The compound's potential medicinal properties and applications in the treatment of various diseases and disorders suggest that it may have significant biological activity, but specific details are not provided in the material.

Toxicity

The toxicity of the compound is not mentioned in the material, and further investigation would be required to determine its safety profile.

Patents and intellectual property

The material does not provide information on any patents or intellectual property related to the compound.

Regulatory status

The regulatory status of the compound, such as its classification as a drug or its approval for use in specific indications, is not provided in the material.

Check Digit Verification of cas no

The CAS Registry Mumber 108664-55-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,6,6 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 108664-55:
(8*1)+(7*0)+(6*8)+(5*6)+(4*6)+(3*4)+(2*5)+(1*5)=137
137 % 10 = 7
So 108664-55-7 is a valid CAS Registry Number.

108664-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-(4-chlorophenyl)-2-oxoethyl)pyridin-2(1H)-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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:108664-55-7 SDS

108664-55-7Relevant academic research and scientific papers

Synthesis and Antifungal Activity of a Series of Novel 1,2-Disubstituted Propenones

Ogata, Masaru,Matsumoto, Hiroshi,Kida, Shiro,Shimizu, Sumio,Tawara, Katsuya,Kawamura, Yoshimi

, p. 1497 - 1502 (2007/10/02)

To find an antifungal agent other than those of the imidazole and triazole series, a new class of 1,2-disubstituted propenones I and II was prepared and tested for antifungal activity.Comparison of the structure-activity relationships showed that the conjugated structure of carbonyl and exomethylene groups in I and II plays an important role in potent antifungal acivity.However, it is noteworthy that compounds 53, 54, and 56, which have a hydroxymethyl or methoxymethyl group instead of an exo-methylene group in I, also showed potent activity.Although many compounds exhibited strong antifungal activity in vitro, none showed activity in vivo of oral efficacy against subacute systemic candidiasis in mice. '

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