Agn-PC-0ndgqw

Base Information

Chemical Name:Agn-PC-0ndgqw
CAS No.:395057-56-4
Molecular Formula:C15H14N4O
Molecular Weight:266.302
Hs Code.:
DSSTox Substance ID:DTXSID40449777
Wikidata:Q82269293

Synonyms:AGN-PC-0NDGQW;395057-56-4;DTXSID40449777;2-hydrazino-3-(4-methoxyphenyl)-1,8-naphthyridine

Suppliers and Price of Agn-PC-0ndgqw

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

Total 0 raw suppliers

Chemical Property of Agn-PC-0ndgqw

Chemical Property:

XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:266.11676108
Heavy Atom Count:20
Complexity:306

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C2=C(N=C3C(=C2)C=CC=N3)NN

Technology Process of Agn-PC-0ndgqw

There total 5 articles about Agn-PC-0ndgqw 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: 88.0%

: 474266-27-8
2-chloro-3-(p-methoxyphenyl)-1,8-naphthyridine

: 395057-56-4
2-hydrazino-3-(p-methoxyphenyl)-1,8-naphthyridine

Guidance literature:: With hydrazine hydrate; In ethanol; for 3h; Heating;
DOI:10.1081/SCC-120006009

Reference yield:

: 7521-41-7
2-Aminonicotinaldehyde

: 395057-56-4
2-hydrazino-3-(p-methoxyphenyl)-1,8-naphthyridine

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / piperidine / 0.13 h / 20 °C

2: 75 percent / 2 N HCl; aq. NaNO₂ / 0.5 h / 20 °C

3: 85 percent / POCl₃ / 2 h / Heating

4: 88 percent / N₂H₄*H₂O / ethanol / 3 h / Heating

With piperidine; hydrogenchloride; hydrazine hydrate; sodium nitrite; trichlorophosphate; In ethanol;
DOI:10.1081/SCC-120006009

Reference yield:

: 104-47-2
p-methoxybenzylnitrile

: 395057-56-4
2-hydrazino-3-(p-methoxyphenyl)-1,8-naphthyridine

Guidance literature:: Multi-step reaction with 4 steps

1: 98 percent / piperidine / 0.13 h / 20 °C

2: 75 percent / 2 N HCl; aq. NaNO₂ / 0.5 h / 20 °C

3: 85 percent / POCl₃ / 2 h / Heating

4: 88 percent / N₂H₄*H₂O / ethanol / 3 h / Heating

With piperidine; hydrogenchloride; hydrazine hydrate; sodium nitrite; trichlorophosphate; In ethanol;
DOI:10.1081/SCC-120006009