104941-03-9

Basic information

• Product Name: 1-{(1Z)-1-[(4-chlorophenyl)carbonyl]but-1-en-1-yl}pyridin-2(1H)-one
• CAS NO: 104941-03-9
• Molecular Formula: C₁₆H₁₄ClNO₂
• Molecular Weight: 287.7409
• Mol File: 104941-03-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 478°C at 760 mmHg
• Flash Point: 242.9°C
• Density: 1.256g/cm³
• Vapor Pressure: 2.67E-09mmHg at 25°C
• Refractive Index: 1.604
• CAS DataBase Reference: 1-{(1Z)-1-[(4-chlorophenyl)carbonyl]but-1-en-1-yl}pyridin-2(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-{(1Z)-1-[(4-chlorophenyl)carbonyl]but-1-en-1-yl}pyridin-2(1H)-one(104941-03-9)
• EPA Substance Registry System: 1-{(1Z)-1-[(4-chlorophenyl)carbonyl]but-1-en-1-yl}pyridin-2(1H)-one(104941-03-9)

Safety Data

• Hazardous Substances Data: 104941-03-9(Hazardous Substances Data)

Usage

Explanation

The compound is composed of 17 carbon atoms, 14 hydrogen atoms, 1 chlorine atom, 1 nitrogen atom, and 1 oxygen atom.

Explanation

The compound is derived from a pyridinone, which is a heterocyclic compound containing a pyridine ring fused to a ketone.

Explanation

The compound has a butenyl carbonyl group (a carbonyl group attached to a butenyl group) and a chlorophenyl substituent (a phenyl ring with a chlorine atom).

Explanation

The compound has a Z-configuration at the double bond in the butenyl carbonyl group, which means that the chlorine atom and the carbonyl group are on the same side of the double bond.

Explanation

Due to its structure and functional groups, the compound may have potential biological activities or pharmaceutical applications, which would require further analysis and testing to determine.

Explanation

The compound's potential properties and uses could be relevant in various fields, such as medicine for drug development, chemistry for understanding its reactivity and synthesis, and biochemistry for studying its interactions with biological systems.

Chemical structure

Pyridinone derivative

Functional groups

Butenyl carbonyl and chlorophenyl substituent

Stereochemistry

(1Z)-1-[(4-chlorophenyl)carbonyl]but-1-en-1-yl

Potential applications

Biological activities or pharmaceutical applications

Field of interest

Medicine, chemistry, or biochemistry

Upstream product

• 536-38-9 4-chlorobenzoylmethyl bromide 
• 142-08-5 2-Pyridone 
• 123-38-6 propionaldehyde 
• 108664-55-7 1-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-1H-pyridin-2-one 

Relevant articles and documents

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

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. '