Welcome to LookChem.com Sign In|Join Free
  • or
"2-{[1-(3-ethoxyphenyl)-2,5-dioxopyrrolidin-3-yl]sulfanyl}-N-naphthalen-2-ylacetamide" is a complex organic compound with the molecular formula C21H19NO5S. It features a naphthalene-2-ylacetamide group, a pyrrolidine ring with a sulfanyl group, and an ethoxyphenyl moiety. 2-{[1-(3-ethoxyphenyl)-2,5-dioxopyrrolidin-3-yl]sulfanyl}-N-naphthalen-2-ylacetamide is characterized by its unique structure, which includes a pyrrolidine ring in a 2,5-dioxo configuration, indicating the presence of two oxygen atoms in the ring, likely in the form of carbonyl groups. The ethoxyphenyl group attached to the pyrrolidine ring introduces an ether linkage and a phenyl ring, which can influence the compound's chemical properties. The sulfanyl group provides a sulfur atom with two hydrogen atoms, which can participate in various chemical reactions. 2-{[1-(3-ethoxyphenyl)-2,5-dioxopyrrolidin-3-yl]sulfanyl}-N-naphthalen-2-ylacetamide may have potential applications in pharmaceuticals or as a chemical intermediate due to its intricate structure and functional groups.

5758-12-3

Post Buying Request

5758-12-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

5758-12-3 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

Check Digit Verification of cas no

The CAS Registry Mumber 5758-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5758-12:
(6*5)+(5*7)+(4*5)+(3*8)+(2*1)+(1*2)=113
113 % 10 = 3
So 5758-12-3 is a valid CAS Registry Number.

5758-12-3SDS

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 N-(2,3-dihydroinden-1-ylideneamino)-N-methylmethanamine

1.2 Other means of identification

Product number -
Other names 1-indanone dimethylhydrazone

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:5758-12-3 SDS

5758-12-3Relevant academic research and scientific papers

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

Cao, Min,Yesilcimen, Ahmet,Wasa, Masayuki

supporting information, p. 4199 - 4203 (2019/04/13)

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

Direct spirocyclization from keto-sulfonamides: An approach to azaspiro compounds

Beltran, Frédéric,Fabre, Indira,Ciofini, Ilaria,Miesch, Laurence

supporting information, p. 5042 - 5045 (2017/11/06)

Spontaneous spirocyclization of keto-sulfonamides via ynamides through a one-pot process is presented. Push-pull ynamides were obtained through Michael addition/elimination without Cu. The obtained azaspiro compounds are building blocks for indole alkaloids. Theoretical studies provide insights into the mechanism of the formal Conia-ene reaction.

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

Henin, Francoise,M'Boungou-M'Passi, Athanase,Muzart, Jacques,Pete, Jean-Pierre

, p. 2849 - 2864 (2007/10/02)

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 5758-12-3