36104-60-6

Basic information

• Product Name: 3-(1,3-Dithiolan-2-yl)-1H-indole
• Synonyms: 3-(1,3-Dithiolan-2-yl)-1H-indole;3-(1,3-dithiolan-2-yl)indole
• CAS NO: 36104-60-6
• Molecular Formula: C₁₁H₁₁NS₂
• Molecular Weight: 221.3417
• Mol File: 36104-60-6.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 444.2°Cat760mmHg
• Flash Point: 222.4°C
• Appearance: /
• Density: 1.347g/cm³
• Vapor Pressure: 1.14E-07mmHg at 25°C
• Refractive Index: 1.749
• CAS DataBase Reference: 3-(1,3-Dithiolan-2-yl)-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1,3-Dithiolan-2-yl)-1H-indole(36104-60-6)
• EPA Substance Registry System: 3-(1,3-Dithiolan-2-yl)-1H-indole(36104-60-6)

Safety Data

• Hazardous Substances Data: 36104-60-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H11NS2/c1-2-4-10-8(3-1)9(7-12-10)11-13-5-6-14-11/h1-4,7,11-12H,5-6H2

Upstream product

• 120-72-9 indole 
• 33145-02-7 2,2'-<1,2-ethanediylbis(thio)>bis-1,3-dithiolane 
• 65225-59-4 2-ethoxy-[1,3]dithiolane 
• 487-89-8 Indole-3-carboxaldehyde 
• 540-63-6 ethane-1,2-dithiol 

Downstream Products

• 487-89-8 Indole-3-carboxaldehyde 

Relevant articles and documents

Graphene oxide (GO)-catalyzed chemoselective thioacetalization of aldehydes under solvent-free conditions

An efficient method for the synthesis of open chain, cyclic, and unsymmetrical dithioacetals from aryl/hetero-aryl/aliphatic aldehydes is described. The reaction is performed using graphene oxide (GO) as the catalyst under solvent-free and aerobic conditions. High chemoselectivity is observed in the reaction as aryl/alkyl ketones do not give thioketals under the condition.

Poly(N-bromobenzene-1,3-disulfonamide) and N,N,N′,N′- tetrabromobenzene-1,3-disulfonamide as a mild and efficient catalyst for chemoselective thioacetalization of carbonyl functions and transthioacetalization reactions

Poly(N-bromobenzene-1,3-disulfonamide) and N,N,N′,N′- tetrabromobenzene-1,3-disulfonamide are effective catalysts for chemoselective dithioacetalization of aldehydes in the presence of ketones under neutral conditions.

Comparative radioprotective activity of various pentagonal compounds with two heteroatomes

Various heterocyclic compounds with two heteroatomes were synthesized and their potential radioprotective activity was tested. This study shows the interest of phenylthiazolidines derivatives in chemical radioprotection.