2-Naphthalenecarboxamide, 6-cyano-N-(3-phenoxyphenyl)-

Base Information

Chemical Name:2-Naphthalenecarboxamide, 6-cyano-N-(3-phenoxyphenyl)-
CAS No.:653604-44-5
Molecular Formula:C24H16N2O2
Molecular Weight:364.403
Hs Code.:
DSSTox Substance ID:DTXSID20465632
Wikidata:Q82291759

Synonyms:653604-44-5;2-Naphthalenecarboxamide, 6-cyano-N-(3-phenoxyphenyl)-;DTXSID20465632

Suppliers and Price of 2-Naphthalenecarboxamide, 6-cyano-N-(3-phenoxyphenyl)-

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 1 raw suppliers

Chemical Property of 2-Naphthalenecarboxamide, 6-cyano-N-(3-phenoxyphenyl)-

Chemical Property:

XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:364.121177757
Heavy Atom Count:28
Complexity:576

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)OC2=CC=CC(=C2)NC(=O)C3=CC4=C(C=C3)C=C(C=C4)C#N

Technology Process of 2-Naphthalenecarboxamide, 6-cyano-N-(3-phenoxyphenyl)-

There total 7 articles about 2-Naphthalenecarboxamide, 6-cyano-N-(3-phenoxyphenyl)- 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:

: 68635-22-3
6-Cyano-naphthalene-2-carbonyl chloride

: 3586-12-7
3-phenoxyaniline

: 653604-44-5
6-[N-(3-phenoxyphenyl)carbamyl]-2-naphthalenecarbonitrile

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 20 ℃; for 18h;
DOI:10.1021/jm0300072

Reference yield:

: 5159-60-4
6-cyano-naphthalene-2-carboxylic acid

: 653604-44-5
6-[N-(3-phenoxyphenyl)carbamyl]-2-naphthalenecarbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 99 percent / (COCl)2 / toluene / 22 h / 70 °C

2: Et₃N; DMAP / CH₂Cl₂ / 18 h / 20 °C

With dmap; oxalyl dichloride; triethylamine; In dichloromethane; toluene;
DOI:10.1021/jm0300072

Reference yield:

: 7568-08-3
naphthalene-2,6-dicarboxylic acid monomethyl ester

: 653604-44-5
6-[N-(3-phenoxyphenyl)carbamyl]-2-naphthalenecarbonitrile

Guidance literature:: Multi-step reaction with 6 steps

1: SOCl₂; DMAP / toluene / 1 h / Heating

2: 13.3 g / NH₃(g) / CH₂Cl₂ / 20 °C

3: 94 percent / pyridine; TFAA / dioxane / 3 h / 20 °C

4: 99 percent / aq. LiOH / tetrahydrofuran / 1.5 h / 20 °C

5: 99 percent / (COCl)2 / toluene / 22 h / 70 °C

6: Et₃N; DMAP / CH₂Cl₂ / 18 h / 20 °C

With pyridine; dmap; lithium hydroxide; thionyl chloride; oxalyl dichloride; ammonia; triethylamine; trifluoroacetic anhydride; In tetrahydrofuran; 1,4-dioxane; dichloromethane; toluene;
DOI:10.1021/jm0300072