3-Nitro-1,5-naphthyridin-2(1H)-one

Base Information

Chemical Name:3-Nitro-1,5-naphthyridin-2(1H)-one
CAS No.:64222-33-9
Molecular Formula:C8H5N3O3
Molecular Weight:191.14
Hs Code.:
DSSTox Substance ID:DTXSID80503680
Nikkaji Number:J2.055.518A
Mol file:64222-33-9.mol

Synonyms:3-NITRO-1,5-NAPHTHYRIDIN-2(1H)-ONE;64222-33-9;3-nitro-1H-1,5-naphthyridin-2-one;DTXSID80503680;1,5-Naphthyridin-2(1H)-one, 3-nitro-;AM20061402;FT-0754728;A917627

Suppliers and Price of 3-Nitro-1,5-naphthyridin-2(1H)-one

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

Crysdot
3-Nitro-1,5-naphthyridin-2(1H)-one 95+%
1g
$ 772.00

American Custom Chemicals Corporation
3-NITRO-1,5-NAPHTHYRIDIN-2(1H)-ONE 95.00%
5MG
$ 503.78

Total 8 raw suppliers

Chemical Property of 3-Nitro-1,5-naphthyridin-2(1H)-one

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Refractive Index:1.744
Boiling Point:390.017 °C at 760 mmHg
Flash Point:189.676 °C
Density:1.589 g/cm³
XLogP3:0.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:191.03309103
Heavy Atom Count:14
Complexity:307

Purity/Quality:

97% ^*data from raw suppliers

3-Nitro-1,5-naphthyridin-2(1H)-one 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C=C(C(=O)N2)[N+](=O)[O-])N=C1

Technology Process of 3-Nitro-1,5-naphthyridin-2(1H)-one

There total 3 articles about 3-Nitro-1,5-naphthyridin-2(1H)-one 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: 92.0%

: 38956-59-1
2-acetamido-1,5-naphthyridine

: 64222-33-9
3-nitro-1,5-naphthyridin-2<1H>-one

Guidance literature:: With sulfuric acid; nitric acid; for 4h;
DOI:10.1002/jhet.5570430224

Reference yield:

: 10261-82-2
1,5-naphthyridin-2(1H)-one

: 64222-33-9
3-nitro-1H-[1,5]naphthyridin-2-one

Guidance literature:: With sulfuric acid; sulfur trioxide; nitric acid;
DOI:10.1039/jr9560000212

Reference yield:

: 33630-94-3,954213-74-2
5-amino-2-hydroxypyridine

: 64222-33-9
3-nitro-1H-[1,5]naphthyridin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: H₃aso4; concentrated H₂SO₄

2: H₂SO₄ 3 containing>; HNO₃

With sulfuric acid; sulfur trioxide; nitric acid; orthoarsenic acid;
DOI:10.1039/jr9560000212