5758-12-3

Basic information

• Product Name: 2-{[1-(3-ethoxyphenyl)-2,5-dioxopyrrolidin-3-yl]sulfanyl}-N-naphthalen-2-ylacetamide
• Synonyms: 2-{[1-(3-ethoxyphenyl)-2,5-dioxopyrrolidin-3-yl]sulfanyl}-N-(naphthalen-2-yl)acetamide; Acetamide, 2-[[1-(3-ethoxyphenyl)-2,5-dioxo-3-pyrrolidinyl]thio]-N-2-naphthalenyl-
• CAS NO: 5758-12-3
• Molecular Formula: C₁₁H₁₄N₂
• Molecular Weight: 434.5075
• Mol File: 5758-12-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 771°C at 760 mmHg
• Flash Point: 420.1°C
• Density: 1.35g/cm³
• Vapor Pressure: 1.07E-23mmHg at 25°C
• Refractive Index: 1.685
• CAS DataBase Reference: 2-{[1-(3-ethoxyphenyl)-2,5-dioxopyrrolidin-3-yl]sulfanyl}-N-naphthalen-2-ylacetamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{[1-(3-ethoxyphenyl)-2,5-dioxopyrrolidin-3-yl]sulfanyl}-N-naphthalen-2-ylacetamide(5758-12-3)
• EPA Substance Registry System: 2-{[1-(3-ethoxyphenyl)-2,5-dioxopyrrolidin-3-yl]sulfanyl}-N-naphthalen-2-ylacetamide(5758-12-3)

Safety Data

• Hazardous Substances Data: 5758-12-3(Hazardous Substances Data)

Usage

Molecular weight

479.57 g/mol

Functional groups

sulfanyl group, ethoxyphenyl group, acetamide group

Structure

pyrrolidin-3-yl ring with a sulfanyl group and an ethoxyphenyl group attached, acetamide group with a naphthalen-2-yl ring attached

Potential pharmaceutical applications

due to its complex structure and the presence of sulfanyl and acetamide groups, common in pharmaceutical compounds

Need for further research

to explore potential uses and properties of the compound

Upstream product

• 83-33-0 inden-1-one 
• 57-14-7 N,N-Dimethylhydrazine 

Downstream Products

• 5736-44-7 Indanon-⁽¹⁾-hydrazon 
• 157485-24-0 2-methyl-2-isobutenylindan-1-one 
• 17496-14-9 2,3-dihydro-2-methyl-1H-inden-1-one 
• 83-33-0 inden-1-one 

Relevant articles and documents

Enantioselective Conia-Ene-Type Cyclizations of Alkynyl Ketones through Cooperative Action of B(C6F5)3, N-Alkylamine and a Zn-Based Catalyst

An efficient and highly enantioselective Conia-ene-type process has been developed. Reactions are catalyzed by a combination of B(C6F5)3, an N-alkylamine and a BOX-ZnI2 complex. Specifically, through cooperative

Photoreactivity of α-Tetrasubstituted Arylketones: Production and Asymmetric Tautomerization of Arylenols

In the presence of catalytic amounts of optically active aminoalcohols, the irradiation of α-disubstituted indanones, tetralones and propiophenones bearing at least one hydrogen in the γ-position led to Norrish type II cleavage compounds which were obtained with enantiomeric excesses reaching 89percent.The influence of the reaction conditions (temperature, wavelength of the UV light and nature of the aminoalcohol) has been analyzed.