1756-44-1

Basic information

• Product Name: Aethoxidum
• Synonyms: 2,2'-diethoxythio-carbanilid;2,2'-diethoxythiocarbanilide;Aethoxidum;Ethocarlide;n,n'-bis(2-ethoxyphenyl)-thioure
• CAS NO: 1756-44-1
• Molecular Formula: C₁₇H₂₀N₂O₂S
• Molecular Weight: 0
• Mol File: 1756-44-1.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 441.2°Cat760mmHg
• Flash Point: 220.6°C
• Appearance: /
• Density: 1.222g/cm³
• Vapor Pressure: 5.55E-08mmHg at 25°C
• Refractive Index: 1.655
• CAS DataBase Reference: Aethoxidum(CAS DataBase Reference)
• NIST Chemistry Reference: Aethoxidum(1756-44-1)
• EPA Substance Registry System: Aethoxidum(1756-44-1)

Safety Data

• Hazardous Substances Data: 1756-44-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H20N2O2S/c1-3-20-15-11-7-5-9-13(15)18-17(22)19-14-10-6-8-12-16(14)21-4-2/h5-12H,3-4H2,1-2H3,(H2,18,19,22)

Upstream product

• 56-23-5 tetrachloromethane 
• 94-70-2 ortho-phenitidine 
• 23163-84-0 1-ethoxy-2-isothiocyanato-benzene 
• 75-15-0 carbon disulfide 

Downstream Products

• 109931-12-6 3-(2-ethoxy-phenyl)-2-(2-ethoxy-phenylimino)-5-methyl-thiazolidin-4-one 
• 105910-01-8 3-(2-ethoxy-phenyl)-5-methyl-thiazolidine-2,4-dione 
• 109933-73-5 3-(2-ethoxy-phenyl)-2-(2-ethoxy-phenylimino)-thiazolidin-4-one 
• 102750-14-1 3-(2-ethoxy-phenyl)-2-(2-ethoxy-phenylimino)-5-furfurylidene-thiazolidin-4-one 
• 102081-89-0 3-(2-ethoxy-phenyl)-2-(2-ethoxy-phenylimino)-1,1-dioxo-1λ⁶-thiazolidin-4-one 
• 114398-40-2 5-(2-chloro-benzylidene)-3-(2-ethoxy-phenyl)-2-(2-ethoxy-phenylimino)-thiazolidin-4-one 
• 114696-84-3 3-(2-ethoxy-phenyl)-2-(2-ethoxy-phenylimino)-5-(3-phenyl-allylidene)-thiazolidin-4-one 
• 115207-38-0 3-(2-ethoxy-phenyl)-2-(2-ethoxy-phenylimino)-5-benzylidene-thiazolidin-4-one 
• 114553-22-9 3-(2-ethoxy-phenyl)-2-(2-ethoxy-phenylimino)-thiazolidine-4,5-dione 5-p-tolylhydrazone 
• 96707-59-4 3-(2-ethoxy-phenyl)-2-(2-ethoxy-phenylimino)-thiazolidine-4,5-dione 5-phenylhydrazone 
• 103989-17-9 3-(2-ethoxy-phenyl)-thiazolidine-2,4-dione 

Relevant articles and documents

Novel non-peptidic small molecule inhibitors of secreted aspartic protease 2 (SAP2) for the treatment of resistant fungal infections

Targeting secreted aspartic protease 2 (SAP2), a kind of virulence factor, represents a new strategy for antifungal drug discovery. In this report, the first-generation of small molecule SAP2 inhibitors was rationally designed and optimized using a structure-based approach. In particular, inhibitor 23h was highly potent and selective and showed good antifungal potency for the treatment of resistant Candida albicans infections.

Applications of Phase Transfer Catalysis, 26. - Thioureas by Three-Component Reactions of Amines, Carbon Tetrachloride, and Sulfide Ions

The title reactions proceed exothermically in the presence of a phase transfer catalyst.Thiophosgene is an intermediate in this conversion, and its phase transfer catalytic transformation into carbon disulfide and trithiocarbonate can be demonstrated.Perchloromethanethiol/sodium sulfide and a PT catalyst yield thiophosgene too.Activated vicinal dibromides were debrominated by Na2S/catalyst.