34755-95-8

Basic information

• Product Name: N-[(E)-thiophen-2-ylmethylidene]naphthalen-2-amine
• CAS NO: 34755-95-8
• Molecular Formula: C₁₅H₁₁NS
• Molecular Weight: 237.3195
• Mol File: 34755-95-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 409.6°C at 760 mmHg
• Flash Point: 201.5°C
• Density: 1.14g/cm³
• Vapor Pressure: 1.52E-06mmHg at 25°C
• Refractive Index: 1.64
• CAS DataBase Reference: N-[(E)-thiophen-2-ylmethylidene]naphthalen-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(E)-thiophen-2-ylmethylidene]naphthalen-2-amine(34755-95-8)
• EPA Substance Registry System: N-[(E)-thiophen-2-ylmethylidene]naphthalen-2-amine(34755-95-8)

Safety Data

• Hazardous Substances Data: 34755-95-8(Hazardous Substances Data)

Upstream product

• 98-03-3 thiophene-2-carbaldehyde 
• 91-59-8 naphthalen-2-ylamine 

Downstream Products

• 22319-92-2 1-(4-chloro-phenyl)-3-thiophen-2-yl-benzo[f]quinoline 
• 22319-72-8 1-(4-bromo-phenyl)-3-thiophen-2-yl-benzo[f]quinoline 
• 36710-57-3 1-phenyl-3-thiophen-2-yl-benzo[f]quinolin-2-ylamine 
• 22319-71-7 1-phenyl-3-thiophen-2-yl-benzo[f]quinoline 
• 22319-74-0 1-(4-ethoxy-phenyl)-3-thiophen-2-yl-benzo[f]quinoline 
• 22319-73-9 1-(4-methoxy-phenyl)-3-thiophen-2-yl-benzo[f]quinoline 
• 713095-56-8 3,3-dimethyl-9-(2-thiophenyl)-1,2,3,4,9,10-hexahydrobenzo[a]acridine-1-one 
• 1049682-56-5 2-phenyl-3-(2-thiophenyl)-benzo[f]quinoline 

Relevant articles and documents

Rhodium-Catalyzed Dehydrogenative Annulation of N-Arylmethanimines with Vinylene Carbonate for Synthesizing Quinolines

Here we report a novel Rh-catalyzed C-H/C-H alkenylation of N-arylmethanimines with vinylene carbonate acting as a vinylene unit. Forty examples of C3,C4-nonsubstituted quinolines were achieved from commercially available starting materials. This identified process features an exceedingly simple system, a lower loading of catalyst, and the capacity for postfunctionalization with bioactive molecules.

A stereoselective Povarov reaction leading to exo-tetrahydroindolo[3,2-c] quinoline derivatives catalyzed by iodine

We report an iodine-catalyzed Povarov reaction using indole as dienophile carried out in toluene at room temperature. This three-component reaction, coupling an aldehyde, an amine, and an indole, proved to be an efficient method for synthesizing exo-indol