6-Methoxy-3-nitroquinoline

Base Information

Chemical Name:6-Methoxy-3-nitroquinoline
CAS No.:159454-73-6
Molecular Formula:C10H8N2O3
Molecular Weight:204.1821
Hs Code.:2933499090
DSSTox Substance ID:DTXSID70364020
Wikidata:Q82147792
Mol file:159454-73-6.mol

Synonyms:6-methoxy-3-nitroquinoline;159454-73-6;6-Methoxy-3-nitro-quinoline;3-nitro-6-methoxyquinoline;SCHEMBL2815910;DTXSID70364020;MFCD06411221;STK664875;AKOS003388212;SB69024;LS-08482

Suppliers and Price of 6-Methoxy-3-nitroquinoline

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

Matrix Scientific
6-Methoxy-3-nitroquinoline
1g
$ 300.00

Matrix Scientific
6-Methoxy-3-nitroquinoline
0.500g
$ 240.00

Matrix Scientific
6-Methoxy-3-nitroquinoline
5g
$ 1000.00

Crysdot
6-Methoxy-3-nitroquinoline 95+%
1g
$ 535.00

Chemenu
6-Methoxy-3-nitroquinoline 95%
1g
$ 505.00

American Custom Chemicals Corporation
6-METHOXY-3-NITROQUINOLINE 95.00%
5MG
$ 495.62

Alichem
6-Methoxy-3-nitroquinoline
1g
$ 475.24

AK Scientific
6-Methoxy-3-nitroquinoline
1g
$ 455.00

Total 5 raw suppliers

Chemical Property of 6-Methoxy-3-nitroquinoline

Chemical Property:

Vapor Pressure:5.94E-05mmHg at 25°C
Boiling Point:356.6°C at 760 mmHg
PKA:1.19±0.14(Predicted)
Flash Point:169.5°C
PSA：67.94000
Density:1.337g/cm³
LogP:2.67480
Storage Temp.:2-8°C
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:204.05349212
Heavy Atom Count:15
Complexity:241

Purity/Quality:

95+% ^*data from raw suppliers

6-Methoxy-3-nitroquinoline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=CC(=CN=C2C=C1)[N+](=O)[O-]

Technology Process of 6-Methoxy-3-nitroquinoline

There total 9 articles about 6-Methoxy-3-nitroquinoline 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: 48.0%

: 159454-58-7
(E)-3-(4-Methoxy-phenylamino)-2-nitro-propenal

: 159454-73-6
3-nitro-6-methoxyquinoline

Guidance literature:: With p-anisidine hydrochloride; thiophenol; In acetic acid; Heating;
DOI:10.1021/ja970435v

Reference yield: 48.0%

: 53094-53-4
(E)-3-(4-Methoxy-phenylamino)-2-nitro-propenal

: 159454-73-6
3-nitro-6-methoxyquinoline

Guidance literature:: With 3,5-Dimethylthiophenol; acetic acid; Heating;
DOI:10.1039/c39940001543

Reference yield: 25.0%

: 609-32-5
2-nitromalonaldehyde

: 20265-97-8
p-anisidine hydrochloride

: 104-94-9
4-methoxy-aniline

: 159454-73-6
3-nitro-6-methoxyquinoline

Guidance literature:: 2-nitromalonaldehyde; 4-methoxy-aniline; With hydrogenchloride; In water; for 0.166667h;

p-anisidine hydrochloride; With acetic acid; In water; for 0.333333h; Inert atmosphere; Reflux;

With thiophenol; In water; for 50h; Reflux; Inert atmosphere;