N-(2,3-Dihydro-1-oxo-6-phenoxy-1H-inden-5-yl)acetamide

Base Information

Chemical Name:N-(2,3-Dihydro-1-oxo-6-phenoxy-1H-inden-5-yl)acetamide
CAS No.:82505-50-8
Molecular Formula:C₁₇H₁₅NO₃
Molecular Weight:281.311
Hs Code.:
DSSTox Substance ID:DTXSID801209849

Synonyms:N-(2,3-Dihydro-1-oxo-6-phenoxy-1H-inden-5-yl)acetamide;DTXSID801209849;82505-50-8

Suppliers and Price of N-(2,3-Dihydro-1-oxo-6-phenoxy-1H-inden-5-yl)acetamide

Supply Marketing:

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

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Chemical Property of N-(2,3-Dihydro-1-oxo-6-phenoxy-1H-inden-5-yl)acetamide

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:281.10519334
Heavy Atom Count:21
Complexity:403

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)NC1=C(C=C2C(=C1)CCC2=O)OC3=CC=CC=C3

Technology Process of N-(2,3-Dihydro-1-oxo-6-phenoxy-1H-inden-5-yl)acetamide

There total 1 articles about N-(2,3-Dihydro-1-oxo-6-phenoxy-1H-inden-5-yl)acetamide 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:

: 108-24-7
acetic anhydride

: 75370-07-9
6-Phenoxy-5-indanylamin

: 82505-50-8
N-(1-Oxo-6-phenoxy-5-indanyl)-acetamide

: 82505-52-0
N-(1-Oxo-5-phenoxy-6-indanyl)-acetamide

Guidance literature:: With chromium(III) oxide; Yield given. Multistep reaction. Yields of byproduct given; 1.) AcOH, 25 deg C, 30 min; 2.) AcOH, water, 40 deg C, 2 h;

Reference yield: 97.0%

: 82505-50-8
N-(1-Oxo-6-phenoxy-5-indanyl)-acetamide

: 75360-80-4
5-Amino-6-phenoxy-1-indanone

Guidance literature:: With hydrogenchloride; In ethanol; for 2h; Heating;

Reference yield:

: 82505-50-8
N-(1-Oxo-6-phenoxy-5-indanyl)-acetamide

: 82505-63-3
N-(3-Methyl-6-phenoxy-5-indanyl)-methansulfonamid

Guidance literature:: Multi-step reaction with 5 steps

1: 97 percent / 10 N HCl / ethanol / 2 h / Heating

2: 82 percent / pyridine / 1.) 0 deg C, 1 h; 2.) 20 deg C, 2 h

3: 54 percent / tetrahydrofuran; diethyl ether / 1.) 40 deg C, 6 h; 2.) 20 deg C, 16 h

4: 85 percent / p-toluenesulfonic acid / acetone / 0.5 h

5: 90 percent / H₂ / Pd-C / dioxane; ethanol

With hydrogenchloride; hydrogen; toluene-4-sulfonic acid; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; pyridine; diethyl ether; ethanol; acetone;