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136573-96-1

INDOLOQUINOLIZINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 136573-96-1 Structure

  • Basic information

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

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: INDOLOQUINOLIZINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: INDOLOQUINOLIZINE(136573-96-1)
    11. EPA Substance Registry System: INDOLOQUINOLIZINE(136573-96-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 136573-96-1(Hazardous Substances Data)

136573-96-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136573-96-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,5,7 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136573-96:
(8*1)+(7*3)+(6*6)+(5*5)+(4*7)+(3*3)+(2*9)+(1*6)=151
151 % 10 = 1
So 136573-96-1 is a valid CAS Registry Number.

136573-96-1Downstream Products

136573-96-1Related 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

136573-96-1Relevant articles and documents

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

Mangeney,Gosmini,Raussou,Commercon,Alexakis

, p. 1877 - 1888 (2007/10/02)

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

Enantioselective Synthesis of Indoloquinolizidines. Key words: Chiral 1,4-dihydropyridines - chiral symmetrical diamines - chiral indoloquinolizidines.

Mangeney, Pierre,Gosmini, Romain,Alexakis, Alexandre

, p. 3981 - 3984 (2007/10/02)

Asymmetric synthesis of indoloquinolizidine has been accomplished by using acyl pyridinium salt bearing in 3 position a chiral aminal.

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