1-(2-AMINOPHENOXY)NAPHTHALENE

Base Information

Chemical Name:1-(2-AMINOPHENOXY)NAPHTHALENE
CAS No.:32219-16-2
Molecular Formula:C16H13NO
Molecular Weight:235.285
Hs Code.:
Mol file:32219-16-2.mol

Synonyms:2-(Naphthalen-1-yloxy)-phenylamine;

Suppliers and Price of 1-(2-AMINOPHENOXY)NAPHTHALENE

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-(1-Naphthyloxy)aniline
500mg
$ 205.00

American Custom Chemicals Corporation
1-(2-AMINOPHENOXY)NAPHTHALENE 95.00%
500MG
$ 802.73

Total 4 raw suppliers

Chemical Property of 1-(2-AMINOPHENOXY)NAPHTHALENE

Chemical Property:

PSA：35.25000
LogP:4.79550

Purity/Quality:

98%min ^*data from raw suppliers

2-(1-Naphthyloxy)aniline ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi

MSDS Files:

Useful:

Technology Process of 1-(2-AMINOPHENOXY)NAPHTHALENE

There total 3 articles about 1-(2-AMINOPHENOXY)NAPHTHALENE 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: 97.0%

: 32219-13-9
1-(2-nitrophenoxy)naphthalene

: 32219-16-2
1-(2-aminophenoxy)naphthalene

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In ethanol; at 20 ℃; for 25h;
DOI:10.1002/poc.3505

Reference yield:

: 1493-27-2,127723-77-7
ortho-nitrofluorobenzene

: 32219-16-2
1-(2-aminophenoxy)naphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / toluene / Inert atmosphere; Reflux

2: hydrogenchloride; iron / water; ethanol / Inert atmosphere; Reflux

With hydrogenchloride; iron; potassium carbonate; In ethanol; water; toluene;
DOI:10.1021/acs.orglett.7b01726

Reference yield:

: 88-73-3
2-Chloronitrobenzene

: 32219-16-2
1-(2-aminophenoxy)naphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: potassium hydroxide / dimethyl sulfoxide / 7 h / 90 °C

2: palladium 10% on activated carbon; hydrogen / ethanol / 25 h / 20 °C

With palladium 10% on activated carbon; hydrogen; potassium hydroxide; In ethanol; dimethyl sulfoxide;
DOI:10.1002/poc.3505