2,6-Naphthyridine

Base Information

Chemical Name:2,6-Naphthyridine
CAS No.:253-50-9
Molecular Formula:C₈H₆N₂
Molecular Weight:130.149
Hs Code.:2933990090
European Community (EC) Number:874-939-7
DSSTox Substance ID:DTXSID40179941
Nikkaji Number:J480.648D
Wikidata:Q27116909
Metabolomics Workbench ID:55444
Mol file:253-50-9.mol

Synonyms:2,6-Naphthyridine;253-50-9;CHEBI:36630;2,6-Naphthyridine(7CI,8CI,9CI);SCHEMBL152013;DTXSID40179941;MFCD06637694;AKOS025395103;AB93197;AS-60286;CS-0157270;W16837;EN300-1387059;Q27116909;Z1255356832

Suppliers and Price of 2,6-Naphthyridine

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
2,6-Naphthyridine 95%
5g
$ 3238.00

Matrix Scientific
2,6-Naphthyridine 95%
1g
$ 2158.00

Ambeed
2,6-Naphthyridine 95+%
1g
$ 484.00

Ambeed
2,6-Naphthyridine 95+%
250mg
$ 185.00

Ambeed
2,6-Naphthyridine 95+%
100mg
$ 130.00

AccelPharmtech
2,6-Naphthyridine 97.00%
25G
$ 6000.00

AccelPharmtech
2,6-Naphthyridine 97.00%
1G
$ 1890.00

Total 8 raw suppliers

Chemical Property of 2,6-Naphthyridine

Chemical Property:

Vapor Pressure:0.00453mmHg at 25°C
Melting Point:114-115 °C
Boiling Point:286.5°C at 760 mmHg
PKA:4.00±0.10(Predicted)
Flash Point:108°C
PSA：25.78000
Density:1.183g/cm³
LogP:1.62980
Storage Temp.:Sealed in dry,Room Temperature
XLogP3:1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:130.053098200
Heavy Atom Count:10
Complexity:99.8

Purity/Quality:

97% ^*data from raw suppliers

2,6-Naphthyridine 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CN=CC2=C1C=NC=C2

Technology Process of 2,6-Naphthyridine

There total 9 articles about 2,6-Naphthyridine 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%

: 222167-62-6
3-(trimethylsilylethynyl)pyridine-4-carboxaldehyde

: 253-50-9
2,6-naphthyridine

Guidance literature:: With ammonia; In ethanol; at 80 ℃; for 2h;
DOI:10.1055/s-1999-3379

Reference yield: 71.0%

: 80935-78-0
1-chloro-[2,6]naphthyridine

: 253-50-9
2,6-naphthyridine

Guidance literature:: With hydrogen; sodium acetate; palladium on activated charcoal; In methanol; for 0.166667h; under 2068.6 Torr;

Reference yield:

: 70201-43-3
3-bromo-pyridine-4-carbaldehyde

: 253-50-9
2,6-naphthyridine

Guidance literature:: Multi-step reaction with 2 steps

1: 42 percent / Et₃N / Pd(PPh₃)2Cl₂, CuI / dimethylformamide / 2 h / Ambient temperature

2: 92 percent / NH₃ / ethanol / 2 h / 80 °C

With ammonia; triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1055/s-1999-3379