136573-96-1

Basic information

• Product Name: INDOLOQUINOLIZINE
• Synonyms: INDOLOQUINOLIZINE;(2R,12BS)-2-ETHYL-1,2,6,7,12,12B-HEXAHYDRO-INDOLO[2,3-A]QUINOLIZINE-3-CARBALDEHYDE
• CAS NO: 136573-96-1
• Molecular Formula: C15H10N2
• Molecular Weight: 218.25
• Mol File: 136573-96-1.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: INDOLOQUINOLIZINE(CAS DataBase Reference)
• NIST Chemistry Reference: INDOLOQUINOLIZINE(136573-96-1)
• EPA Substance Registry System: INDOLOQUINOLIZINE(136573-96-1)

Safety Data

• Hazardous Substances Data: 136573-96-1(Hazardous Substances Data)

Upstream product

• 133621-67-7 4-Ethyl-1-<1(H)-indol-3-ylacetyl>-3-(1,3-dimethyl-4,5-diphenylimidazolidin-2-yl)-1,4-dihydropyridine 
• 50720-05-3 indolyl acetyl chloride 
• 136573-95-0 4-Ethyl-1-<2-(1(H)-indol-3-yl)-ethyl>-3-(1,3-dimethyl-4,5-diphenylimidazolidin-2-yl)-1,4-dihydropyridine 
• 133634-31-8 3-(1,3-Dimethyl-4(S),5(S)-diphenylimidazolidin-2-yl)pyridine 
• 22751-68-4 (S,S)-N,N'-dimethyl-1,2-diphenylethane-1,2-diamine 
• 500-22-1 3-pyridinecarboxaldehyde 
• 154819-54-2 (R)-4-Ethyl-1-[2-(1H-indol-3-yl)-ethyl]-1,4-dihydro-pyridine-3-carbaldehyde 
• 136591-52-1 (2R,12bS)-3-((4S,5S)-1,3-Dimethyl-4,5-diphenyl-imidazolidin-2-yl)-2-ethyl-1,2,6,7,12,12b-hexahydro-indolo[2,3-a]quinolizine 
• 917-54-4 methyllithium 
• 10313-60-7 3,4-dimethoxyphenylacetyl chloride 

Related news

Fluorescence resonance energy transfer from a bio-active imidazole derivative 2-(1-phenyl-1H-imidazo[4,5-f][1,10]phenanthrolin-2-yl)phenol to a bioactive INDOLOQUINOLIZINE (cas 136573-96-1) system09/05/2019

Novel donor imidazole derivative, 2-(1-phenyl-1H-imidazo [4,5-f][1,10]phenanthrolin-2-yl)-phenol (PIPP) was screened as highly sensitive chemisensor for transition metal ions and it can be used as a “multi-way” optically switchable material. Solvatochromic effects on the fluorescence behaviour...detailed

Relevant articles and documents

Preparation and utilization of chiral dihydropyridines. Synthesis of chiral indoloquinolizines and benzoquinolizines

An asymmetric synthesis of 3-formyl-1,4-dihydropyridines is described that entails the addition of organocopper reagents to activated 3- imidazolidinylpyridine, prepared with chiral diamines. The activator can be a chloroformate or an acid chloride. The m