100820-45-9

Basic information

• Product Name: trans-5-phenyl-3,4,4a,5,6,10b-hexahydro-2H-pyrano[3,2-c]-quinoline
• CAS NO: 100820-45-9
• Molecular Weight: 265.355
• Mol File: 100820-45-9.mol

Chemical Properties

• CAS DataBase Reference: trans-5-phenyl-3,4,4a,5,6,10b-hexahydro-2H-pyrano[3,2-c]-quinoline(CAS DataBase Reference)
• NIST Chemistry Reference: trans-5-phenyl-3,4,4a,5,6,10b-hexahydro-2H-pyrano[3,2-c]-quinoline(100820-45-9)
• EPA Substance Registry System: trans-5-phenyl-3,4,4a,5,6,10b-hexahydro-2H-pyrano[3,2-c]-quinoline(100820-45-9)

Safety Data

• Hazardous Substances Data: 100820-45-9(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 538-51-2 benzylidene phenylamine 
• 1750-36-3 (E)-N-benzylidenebenzenamine 
• 100-52-7 benzaldehyde 
• 62-53-3 aniline 
• 142-68-7 TETRAHYDROPYRANE 
• 100-46-9 benzylamine 

Relevant articles and documents

A theoretical and experimental study to unequivocal structural assignment of tetrahydroquinoline derivatives

The tetrahydroquinoline derivatives can be easily synthesized through Povarov reaction and have several important biological activities. This work describes a comparative study for the unequivocal assignment of molecular structure of different tetrahydroq

One-pot synthesis of pyrano- and furanoquinolines catalyzed by molten tetra-n-butylphosphonium bromide under solvent-free conditions

Molten tetra-n-butylphosphonium bromide is found to be a practical and inexpensive catalytic media for stereoselective one-pot synthesis of pyranoquinoline and furanoquinoline derivatives in good to excellent yields. Products of undesirable reactions resu

Indium trichloride-catalyzed imino Diels-Alder reactions: Synthesis of new indolylquinoline derivatives

Imino Diels-Alder reaction of N-arylaldimines with cyclopentadiene, 3,4- dihydro-2H-pyran and indene is efficiently catalyzed by indium trichloride to give new indolylquinoline derivatives in good yields.

Proline triflate catalysed Diels-Alder reaction in the synthesis of tetrahydroquinoline derivatives

Proline triflate was found to catalyse efficiently the one-pot synthesis of 2H-pyranotetrahydroquinolines from aryl imines, and 3,4-dihydro-2H-pyran with high stereoselectivity. The aryl imines were formed in situ from aromatic amines and arylaldehydes.

Ceric Ammonium Nitrate (CAN)-Catalyzed, Efficient, One-Pot, Three-Component, aza-Diels-Alder Reactions for a Facile Synthesis of Tetrahydropyranoquinoline Derivatives

A simple, efficient, and cost-effective method for the synthesis of tetrahydropyranoquinoline derivatives by a one-pot condensation of aromatic aldehyde, aromatic amine, and 3,4-dihydro-2H-pyran respectively in the presence of ceric ammonium nitrate (CAN)

Lithium perchlorate/diethylether catalyzed aza-Diels-Alder reaction: An expeditious synthesis of pyrano, indeno quinolines and phenanthridines

Lithium perchlorate in diethylether (LPDE) is found to catalyze imino-Diels-Alder reactions of N-aryl aldimines with 3,4dihydro-2H-pyran (DHP), indene, and cyclohexenone to afford the corresponding pyrano, indeno quinolines and phenanthridinone derivative

Parallel synthesis of polysubstituted tetrahydroquinolines

A three-component cycloaddition was used to prepare a library of polysubtituted tetrahydroquinolines. Reaction conditions were optimised and a large range of anilines, aldehydes and alkenes were tested.

Ferric sulfate [Fe2(SO4)3·xH 2O]: An efficient heterogeneous catalyst for the synthesis of tetrahydroquinoline derivatives using Povarov reaction

Fe2(SO4)3·xH2O can be used as an efficient and reusable catalyst for the synthesis of pyrano- and furanotetrahydroquinolines via one-pot three-component Povarov reaction involving aromatic aldehydes, aromatic am

Convenient synthesis of pyrano[3,2-c]quinolines and indeno[2,1- c]quinolines by imino Diels-Alder reactions

Anhydrous indium trichloride (InCl3) is found to catalyze the imino Diels-Alder reaction of 3,4-dihydro-2H-pyran and indene with Schiff's bases to afford pyrano[3,2-c]quinolines and indeno[2,1-c]quinolines. Imino Diels- Alder reactions of N-ben

CYCLOADDITION REACTIONS OF 3,4-DIHYDRO-2H-PYRAN WITH BENZYLIDENEANILINES

The cycloaddition of dihydropyran to benzylideneaniline and to other anils gives tetrahydroquinolines resulting from addition; contrary to a recent report, there is no evidence for the formation of adducts.