51050-85-2

Basic information

• Product Name: 1H-Indole, 1-ethenyl-4,5,6,7-tetrahydro-
• CAS NO: 51050-85-2
• Molecular Formula: C10H13N
• Molecular Weight: 147.22
• Mol File: 51050-85-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 1-ethenyl-4,5,6,7-tetrahydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 1-ethenyl-4,5,6,7-tetrahydro-(51050-85-2)
• EPA Substance Registry System: 1H-Indole, 1-ethenyl-4,5,6,7-tetrahydro-(51050-85-2)

Safety Data

• Hazardous Substances Data: 51050-85-2(Hazardous Substances Data)

Upstream product

• 100-64-1 cyclohexanone-oxime 
• 593-60-2 Vinyl bromide 
• 75-01-4 chloroethylene 
• 107-06-2 1,2-dichloro-ethane 
• 74-86-2 acetylene 
• 106-93-4 ethylene dibromide 

Downstream Products

• 125188-57-0 1-(1-p-Tolyloxy-ethyl)-4,5,6,7-tetrahydro-1H-indole 
• 125188-60-5 1-[1-(4-Fluoro-phenoxy)-ethyl]-4,5,6,7-tetrahydro-1H-indole 
• 131303-06-5 1-(1-Phenylthioethyl)-4,5,6,7-tetrahydroindole 
• 1619929-26-8 5-phenyl-3-(1-vinyl-4,5,6,7-tetrahydro-1H-indol-2-yl)-4,5-dihydroisoxazol-5-ol 
• 1619929-41-7 2-(5-phenylisoxazol-3-yl)-1-vinyl-4,5,6,7-tetrahydro-1H-indole 
• 13618-91-2 4,5,6,7-tetrahydroindole 
• 120-72-9 indole 
• 62372-28-5 1-ethyl-4,5,6,7-tetrahydroindole 
• 125188-58-1 1-[1-(2-Chloro-phenoxy)-ethyl]-4,5,6,7-tetrahydro-1H-indole 
• 131303-07-6 1-<1-(4-Fluorophenylthio)ethyl>-4,5,6,7-tetrahydroindole 
• 131303-04-3 1-<2-(4-Fluorophenylthio)ethyl>-4,5,6,7-tetrahydroindole 

Relevant articles and documents

PYRROLES FROM KETOXIMES AND ACETYLENE. 22. DIHALOETHANES IN PLACE OF ACETYLENE IN REACTIONS WITH CYCLOHEXANONE OXIME

4,5,6,7-Tetrahydroindole and its 1-vinyl derivative were obtained in overall yields of 30-60percent by the reaction of cyclohexanone oxime with 1,2-dichloro- and 1,2-dibromoethane in the MOH-dimethyl sulfoxide (DMSO) superbase system (M = K, Na, Li).Nucle

PYRROLES FROM KETOXIMES AND ACETYLENE. CONDITIONS OF REACTION OF CYCLOHEXANONE OXIME WITH VINYL HALIDES IN SUPERBASIC MEDIA

4,5,6,7-Tetrahydroindole and its N-vinyl derivatives were synthesized with an overall yield of up to 60percent by the reaction of cyclohexanone oxime with vinyl halides (CH2=CHX, where X = Cl, Br) in a MOH (M = Na, K)-polar aprotic solvent system at 84-140 deg C and atmospheric pressure.