Indolo[2,3-a]quinolizine

Base Information

Chemical Name:Indolo[2,3-a]quinolizine
CAS No.:239-15-6
Molecular Formula:C15H10N2
Molecular Weight:218.25300
Hs Code.:2933990090
DSSTox Substance ID:DTXSID50552983
Nikkaji Number:J2.321.378H,J10.934G
Wikidata:Q82433435
Mol file:239-15-6.mol

Synonyms:Indolo[2,3-a]quinolizine;239-15-6;SCHEMBL3112229;DTXSID50552983

Suppliers and Price of Indolo[2,3-a]quinolizine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
INDOLOQUINOLIZINE 95.00%
5MG
$ 505.48

Total 5 raw suppliers

Chemical Property of Indolo[2,3-a]quinolizine

Chemical Property:

PSA：17.30000
LogP:3.64070
XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:218.084398327
Heavy Atom Count:17
Complexity:360

Purity/Quality:

99% ^*data from raw suppliers

INDOLOQUINOLIZINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C3C=CN4C=CC=CC4=C3N=C2C=C1

Technology Process of Indolo[2,3-a]quinolizine

There total 9 articles about Indolo[2,3-a]quinolizine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 89.0%

: 115438-93-2
12-Benzenesulfonyl-7-hydroxy-6,12-dihydro-7H-indolo[2,3-a]quinolizin-5-ylium; bromide

: 239-15-6
indolo[2,3-a]quinolizine

Guidance literature:: With sodium hydroxide; In methanol; for 4h;
DOI:10.1016/S0040-4039(00)96702-9

Reference yield: 65.0%

: 73282-12-9
1-phenylsulfonyl-2-(pyridin-2-yl)-1H-indole

: 17157-48-1
bromoacetaldehyde

: 239-15-6
indolo[2,3-a]quinolizine

Guidance literature:: Multistep reaction;
DOI:10.1016/j.tet.2006.03.085

Reference yield:

: 13228-40-5
2-(2-pyridinyl)-1H-indole

: 239-15-6
indolo[2,3-a]quinolizine

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / sodium hydride / tetrahydrofuran / 0 - 10 °C

With sodium hydride; In tetrahydrofuran;
DOI:10.1016/j.tet.2006.03.085