N-{2-[(2H-1,3-Benzodioxol-5-yl)oxy]ethyl}benzamide

Base Information

Chemical Name:N-{2-[(2H-1,3-Benzodioxol-5-yl)oxy]ethyl}benzamide
CAS No.:89718-73-0
Molecular Formula:C₁₆H₁₅NO₄
Molecular Weight:285.299
Hs Code.:
DSSTox Substance ID:DTXSID90529432
Wikidata:Q82399847

Synonyms:89718-73-0;N-{2-[(2H-1,3-Benzodioxol-5-yl)oxy]ethyl}benzamide;DTXSID90529432;AKOS028916089;N-(2-(benzo[d][1,3]dioxol-5-yloxy)ethyl)benzamide;F5526-0604;Z435951324

Suppliers and Price of N-{2-[(2H-1,3-Benzodioxol-5-yl)oxy]ethyl}benzamide

Supply Marketing:

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

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Chemical Property of N-{2-[(2H-1,3-Benzodioxol-5-yl)oxy]ethyl}benzamide

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:285.10010796
Heavy Atom Count:21
Complexity:343

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1OC2=C(O1)C=C(C=C2)OCCNC(=O)C3=CC=CC=C3

Technology Process of N-{2-[(2H-1,3-Benzodioxol-5-yl)oxy]ethyl}benzamide

There total 3 articles about N-{2-[(2H-1,3-Benzodioxol-5-yl)oxy]ethyl}benzamide 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: 43.0%

: 72955-85-2
[2-[(Benzodioxol-5-yl)oxy]ethyl]amine

: 98-88-4
benzoyl chloride

: 89718-73-0
N-<2-(1,3-benzodioxol-5-yloxy)ethyl>benzamide

Guidance literature:: With pyridine; In chloroform; for 2h;

Reference yield:

: 533-31-3
Sesamol

: 89718-73-0
N-<2-(1,3-benzodioxol-5-yloxy)ethyl>benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) potassium iodide, 2.) potassium carbonate / 1.) butanone, 18 h, 2.) butanone, reflux, 1.5 h

2: 87 percent / lithium tetrahydroaluminate / diethyl ether / 2 h / Heating

3: 43 percent / pyridine / CHCl₃ / 2 h

With pyridine; lithium aluminium tetrahydride; potassium carbonate; potassium iodide; In diethyl ether; chloroform;

Reference yield:

: 72955-89-6
(1,3-benzodioxol-5-yloxy)ethanenitrile

: 89718-73-0
N-<2-(1,3-benzodioxol-5-yloxy)ethyl>benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / lithium tetrahydroaluminate / diethyl ether / 2 h / Heating

2: 43 percent / pyridine / CHCl₃ / 2 h

With pyridine; lithium aluminium tetrahydride; In diethyl ether; chloroform;