4-(Naphthalen-1-yloxy)aniline

Base Information

Chemical Name:4-(Naphthalen-1-yloxy)aniline
CAS No.:76590-19-7
Molecular Formula:C₁₆H₁₃NO
Molecular Weight:235.285
Hs Code.:
DSSTox Substance ID:DTXSID10356101
Wikidata:Q82135260
Mol file:76590-19-7.mol

Synonyms:4-(naphthalen-1-yloxy)aniline;76590-19-7;4-naphthalen-1-yloxyaniline;4-(1-naphthyloxy)aniline;Benzenamine, 4-(1-naphthalenyloxy)-;1-(4-Aminophenoxy)naphthalene;4-(alpha-Naphthoxy)-aniline;SCHEMBL1177840;[4-(1-naphthyloxy)phenyl]amine;DTXSID10356101;PYGYJLHOEOYGIA-UHFFFAOYSA-N;BBL025900;MFCD01806280;STK662076;AKOS000215318;VS-08139;CS-0322478;FT-0769497

Suppliers and Price of 4-(Naphthalen-1-yloxy)aniline

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

American Custom Chemicals Corporation
1-(4-AMINOPHENOXY)NAPHTHALENE 95.00%
1G
$ 1066.87

Total 5 raw suppliers

Chemical Property of 4-(Naphthalen-1-yloxy)aniline

Chemical Property:

PSA：35.25000
LogP:4.79550
XLogP3:4.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:235.099714038
Heavy Atom Count:18
Complexity:260

Purity/Quality:

99% ^*data from raw suppliers

1-(4-AMINOPHENOXY)NAPHTHALENE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2OC3=CC=C(C=C3)N

Technology Process of 4-(Naphthalen-1-yloxy)aniline

There total 3 articles about 4-(Naphthalen-1-yloxy)aniline 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: 74.0%

: 3402-81-1
1-(4-nitrophenoxy)naphthalene

: 76590-19-7
1-(4-aminophenoxy) naphthalene

Guidance literature:: With 5%-palladium/activated carbon; hydrazine hydrate; In ethanol; for 18h; Inert atmosphere; Reflux;
DOI:10.1155/2015/465286

Reference yield:

: 350-46-9,178603-76-4
4-Fluoronitrobenzene

: 76590-19-7
1-(4-aminophenoxy) naphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / dimethyl sulfoxide / 16 h / Heating; Inert atmosphere

2: tin(II) chloride dihdyrate / ethyl acetate / 16 h / 50 °C / Inert atmosphere

With tin(II) chloride dihdyrate; potassium carbonate; In dimethyl sulfoxide; ethyl acetate;
DOI:10.1016/j.ejmech.2016.02.006

Reference yield:

: 90-15-3
α-naphthol

: 76590-19-7
1-(4-aminophenoxy) naphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / dimethyl sulfoxide / 16 h / Heating; Inert atmosphere

2: tin(II) chloride dihdyrate / ethyl acetate / 16 h / 50 °C / Inert atmosphere

With tin(II) chloride dihdyrate; potassium carbonate; In dimethyl sulfoxide; ethyl acetate;
DOI:10.1016/j.ejmech.2016.02.006