N-(4-Aminoacenaphthen-5-YL)acetamide

Base Information

Chemical Name:N-(4-Aminoacenaphthen-5-YL)acetamide
CAS No.:35341-35-6
Molecular Formula:C14H14N2O
Molecular Weight:226.2738
Hs Code.:
NSC Number:83315
DSSTox Substance ID:DTXSID00292509
Wikidata:Q82030840

Synonyms:35341-35-6;NSC83315;DTXSID00292509;NSC-83315;N-(4-AMINOACENAPHTHEN-5-YL)ACETAMIDE

Suppliers and Price of N-(4-Aminoacenaphthen-5-YL)acetamide

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

Total 3 raw suppliers

Chemical Property of N-(4-Aminoacenaphthen-5-YL)acetamide

Chemical Property:

Vapor Pressure:9.41E-11mmHg at 25°C
Boiling Point:515.9°Cat760mmHg
Flash Point:265.8°C
Density:1.328g/cm³
XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:226.110613074
Heavy Atom Count:17
Complexity:317

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)NC1=C(C=C2CCC3=C2C1=CC=C3)N

Technology Process of N-(4-Aminoacenaphthen-5-YL)acetamide

There total 5 articles about N-(4-Aminoacenaphthen-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: 93.0%

: 4889-61-6
4-nitro-5-acetamidoacenaphthene

: 35341-35-6
4-amino-5-acetamidoacenaphthene

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; for 2h; under 3102.9 Torr;
DOI:10.1021/jo00010a010

Reference yield:

: 602-87-9
4-nitroacenaphthene

: 35341-35-6
4-amino-5-acetamidoacenaphthene

Guidance literature:: Multi-step reaction with 4 steps

1: 91 percent / H₂ / 10percent Pd/C / ethanol / 1 h / 3102.9 Torr

2: 95 percent / pyridine / 0.25 h / Heating

3: 67 percent / Cu(NO₃)2*3H₂O, AcOH / 2 h / 20 °C

4: 93 percent / H₂ / 10percent Pd/C / methanol / 2 h / 3102.9 Torr

With pyridine; hydrogen; copper(II) nitrate; acetic acid; palladium on activated charcoal; In methanol; ethanol;
DOI:10.1021/jo00010a010

Reference yield:

: 4657-93-6
5-aminoacenaphthene

: 35341-35-6
4-amino-5-acetamidoacenaphthene

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / pyridine / 0.25 h / Heating

2: 67 percent / Cu(NO₃)2*3H₂O, AcOH / 2 h / 20 °C

3: 93 percent / H₂ / 10percent Pd/C / methanol / 2 h / 3102.9 Torr

With pyridine; hydrogen; copper(II) nitrate; acetic acid; palladium on activated charcoal; In methanol;
DOI:10.1021/jo00010a010