Ethyl (4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)acetate

Base Information

Chemical Name:Ethyl (4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)acetate
CAS No.:136603-10-6
Molecular Formula:C₂₅H₂₀N₂O₄
Molecular Weight:412.445
Hs Code.:
DSSTox Substance ID:DTXSID90929493
Wikidata:Q82904431

Synonyms:BRN 4887709;Ethyl (4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)acetate;Acetic acid, (4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)-, ethyl ester;136603-10-6;DTXSID90929493;C25-H20-N2-O4;Ethyl [4-(2-phenyl-1,8-naphthyridine-3-carbonyl)phenoxy]acetate

Suppliers and Price of Ethyl (4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)acetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Ethyl (4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)acetate

Chemical Property:

Vapor Pressure:1.6E-15mmHg at 25°C
Boiling Point:624.7°C at 760 mmHg
Flash Point:331.6°C
Density:1.248g/cm³
XLogP3:4.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:8
Exact Mass:412.14230712
Heavy Atom Count:31
Complexity:598

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)COC1=CC=C(C=C1)C(=O)C2=C(N=C3C(=C2)C=CC=N3)C4=CC=CC=C4

Technology Process of Ethyl (4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)acetate

There total 3 articles about Ethyl (4-((2-phenyl-1,8-naphthyridin-3-yl)carbonyl)phenoxy)acetate 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: 65.0%

: 116625-85-5
3-p-Hydroxybenzoyl-2-phenyl-1,8-naphthyridine

: 105-39-5
chloroacetic acid ethyl ester

: 136603-10-6
Ethyl p-(3-benzoyl-2-phenyl-1,8-naphthyridinyl)methoxyacetate

Guidance literature:: With potassium carbonate; In acetone; for 18h; Heating;

Reference yield:

: 7521-41-7
2-Aminonicotinaldehyde

: 136603-10-6
Ethyl p-(3-benzoyl-2-phenyl-1,8-naphthyridinyl)methoxyacetate

Guidance literature:: Multi-step reaction with 2 steps

1: conc. H₂SO₄, glac. AcOH

2: 65 percent / K₂CO₃ / acetone / 18 h / Heating

With sulfuric acid; potassium carbonate; acetic acid; In acetone;

Reference yield:

: 52046-71-6
1-(4-hydroxy-phenyl)-3-phenyl-propane-1,3-dione

: 136603-10-6
Ethyl p-(3-benzoyl-2-phenyl-1,8-naphthyridinyl)methoxyacetate

Guidance literature:: Multi-step reaction with 2 steps

1: conc. H₂SO₄, glac. AcOH

2: 65 percent / K₂CO₃ / acetone / 18 h / Heating

With sulfuric acid; potassium carbonate; acetic acid; In acetone;