68394-64-9

Basic information

• Product Name: 1-phenyl-4,5,6,7-tetrahydro-1H-indole
• Synonyms: 1-phenyl-4,5,6,7-tetrahydro-1H-indole
• CAS NO: 68394-64-9
• Molecular Weight: 197.28
• Mol File: 68394-64-9.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-phenyl-4,5,6,7-tetrahydro-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyl-4,5,6,7-tetrahydro-1H-indole(68394-64-9)
• EPA Substance Registry System: 1-phenyl-4,5,6,7-tetrahydro-1H-indole(68394-64-9)

Safety Data

• Hazardous Substances Data: 68394-64-9(Hazardous Substances Data)

Upstream product

• 52480-49-6 1-Phenyl-1,4,5,6,7,7a-hexahydro-2H-indol-2-one 
• 62-53-3 aniline 
• 74255-58-6 3-phenylcyclohexanospiro-2-oxazolidine 
• 586-96-9 Nitrosobenzene 
• 245432-97-7 2-[(E)-2-(cyclohex-1-en-1-yl)ethenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 620634-96-0 C₆H₉CHCH(BO₂(C(CH₃)2)2) 
• 108-94-1 cyclohexanone 
• 107-21-1 ethylene glycol 
• 16806-93-2 4-oxo-4,5,6,7-tetrahydrobenzofuran 
• 504-02-9 1,3-cylohexanedione 
• 23870-03-3 1-phenyl-1,5,6,7-tetrahydro-indol-4-one 
• 147329-74-6 2-(2-Bromo-1-ethoxy-ethyl)-cyclohexanone 
• 6651-36-1 1-(Trimethylsilyloxy)cyclohexene 

Downstream Products

• 16096-33-6 1-phenyl-1H-indole 

Relevant articles and documents

Access to Fused Pyrroles from Cyclic 1,3-Dienyl Boronic Esters and Arylnitroso Compounds

Complimentary to classical hydroboration and boron-Wittig reactions, a new, efficient access to cyclic 1,3-dienyl boronic esters has been developed via diene or triene metathesis. Subsequently, fused pyrroles were synthesized with a broad substrate scope

Multicomponent reactions in PEG-400: Ruthenium-catalyzed synthesis of substituted pyrroles

An efficient and eco-friendly method for the synthesis of substituted pyrroles has been developed via ruthenium-catalyzed multicomponent reaction of ketone, amine, and ethylene glycol in PEG-400 as solvent medium without using any external ligand. The cat

Synthesis of N-aryl-4,5,6,7-tetrahydroindoles

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