1H-1,2,3-Triazolo[4,5-h]quinoline

Base Information

Chemical Name:1H-1,2,3-Triazolo[4,5-h]quinoline
CAS No.:233-92-1
Molecular Formula:C₉H₆N₄
Molecular Weight:170.173
Hs Code.:
DSSTox Substance ID:DTXSID60457536
Nikkaji Number:J1.790.088I
Wikidata:Q82280409
Mol file:233-92-1.mol

Synonyms:233-92-1;1H-1,2,3-Triazolo[4,5-h]quinoline;2H-triazolo[4,5-h]quinoline;triazoloquinoline;AGN-PC-0NH2BF;SCHEMBL1414448;SCHEMBL9374740;DTXSID60457536;3H-1,2,3-Triazolo[4,5-h]quinoline

Suppliers and Price of 1H-1,2,3-Triazolo[4,5-h]quinoline

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

AccelPharmtech
1H-1,2,3-Triazolo[4,5-h]quinoline 97.00%
25G
$ 29000.00

AccelPharmtech
1H-1,2,3-Triazolo[4,5-h]quinoline 97.00%
5G
$ 15300.00

AccelPharmtech
1H-1,2,3-Triazolo[4,5-h]quinoline 97.00%
1G
$ 5840.00

Total 0 raw suppliers

Chemical Property of 1H-1,2,3-Triazolo[4,5-h]quinoline

Chemical Property:

Melting Point:256-257 °C
Boiling Point:490.1±18.0 °C(Predicted)
PSA：54.46000
Density:1.471±0.06 g/cm3(Predicted)
LogP:1.50610
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:170.059246208
Heavy Atom Count:13
Complexity:196

Purity/Quality:: 1H-1,2,3-Triazolo[4,5-h]quinoline 97.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C3=NNN=C3C=C2)N=C1

Technology Process of 1H-1,2,3-Triazolo[4,5-h]quinoline

There total 11 articles about 1H-1,2,3-Triazolo[4,5-h]quinoline 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: 64.0%

: 486421-29-8
(7-amino-quinolin-8-yl)-carbamic acid ethyl ester

: 233-92-1
[1,2,3]triazolo[4,5-h]quinoline

Guidance literature:: With sodium nitrite; In water; acetic acid; at 0 ℃;
DOI:10.1002/jhet.5570390405

Reference yield: 38.0%

: 116940-60-4
6-Chloro-3H-[1,2,3]triazolo[4,5-h]quinoline

: 233-92-1
triazolo<4,5-h>quinoline

Guidance literature:: With sodium hydroxide; hydrogen; nickel; In ethanol; under 900.07 Torr;

Reference yield:

: 578-66-5
8-amino quinoline

: 233-92-1
[1,2,3]triazolo[4,5-h]quinoline

Guidance literature:: Multi-step reaction with 4 steps

1: 83 percent / tetrahydrofuran / 5 h / 20 °C

2: 30 percent / HNO₃; H₂SO₄ / 0.5 h / 0 °C

3: 98 percent / H₂ / Pd/C / ethyl acetate / 20 °C

4: 64 percent / NaNO₂ / acetic acid; H₂O / 0 °C

With sulfuric acid; hydrogen; nitric acid; sodium nitrite; palladium on activated charcoal; In tetrahydrofuran; water; acetic acid; ethyl acetate;
DOI:10.1002/jhet.5570390405