N-Ethyl-N-phenylnaphthalen-1-amine

Base Information

Chemical Name:N-Ethyl-N-phenylnaphthalen-1-amine
CAS No.:110972-21-9
Molecular Formula:C18H17N
Molecular Weight:247.34
Hs Code.:
DSSTox Substance ID:DTXSID30602278
Wikidata:Q82499260
Mol file:110972-21-9.mol

Synonyms:N-Ethyl-N-phenylnaphthalen-1-amine;110972-21-9;SCHEMBL2185816;DTXSID30602278;YIQQHFQDYLXTPG-UHFFFAOYSA-N;1-(N-phenyl-N-ethylamino)naphthalene;1-(N-ethyl-N-phenylamino)-naphthalene

Suppliers and Price of N-Ethyl-N-phenylnaphthalen-1-amine

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-Ethyl-N-phenylnaphthalen-1-amine

Chemical Property:

XLogP3:5.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:247.136099547
Heavy Atom Count:19
Complexity:269

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN(C1=CC=CC=C1)C2=CC=CC3=CC=CC=C32

Technology Process of N-Ethyl-N-phenylnaphthalen-1-amine

There total 3 articles about N-Ethyl-N-phenylnaphthalen-1-amine 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%

: 110972-21-9
N-ethyl-N-phenyl-1-naphthylamine

Guidance literature:

Reference yield: 28.0%

: 86-57-7
1-Nitronaphthalene

: 103-69-5
N-ethyl-N-phenylamine

: 110972-21-9
N-ethyl-N-phenyl-1-naphthylamine

Guidance literature:: With bis(acetylacetonato)palladium(II); potassium phosphate tribasic trihydrate; 2-(2,6-diethyl-4-methylphenyl)-5-(2,4,6-triisopropylphenyl)imidazo[1,5-a]pyridin-2-ium chloride; In 1,4-dioxane; at 130 ℃; for 24h; Inert atmosphere;
DOI:10.1021/acscatal.9b02760

Reference yield:

: 90-30-2
N-phenyl-1-naphthylamine

: 110972-21-9
N-ethyl-N-phenyl-1-naphthylamine

Guidance literature:: With triethyloxonium fluoroborate; phenyllithium; Yield given. Multistep reaction; 1.) cyclohexane, ether, -30 deg C, 2.) cyclohexane, ether, RT, overnight;
DOI:10.1021/jo00236a036