Phthalimide, N-(5-(p-aminophenoxy)pentyl)-3-nitro-

Base Information

• Chemical Name: Phthalimide, N-(5-(p-aminophenoxy)pentyl)-3-nitro-
• CAS No.: 108368-14-5
• Molecular Formula: C₁₉H₁₉N₃O₅
• Molecular Weight: 369.377
• DSSTox Substance ID: DTXSID50148527
• Wikidata: Q83014075
• Mol file: 108368-14-5.mol

Synonyms:Phthalimide, N-(5-(p-aminophenoxy)pentyl)-3-nitro-;108368-14-5;M & B 3693;BRN 0345251;N-(5-(p-Aminophenoxy)pentyl)-3-nitrophthalimide;4-21-00-05418 (Beilstein Handbook Reference);2-[5-(4-aminophenoxy)pentyl]-4-nitroisoindole-1,3-dione;DTXSID50148527;AKOS040753550;LS-109429

Chemical Property of Phthalimide, N-(5-(p-aminophenoxy)pentyl)-3-nitro-

Chemical Property:

• Vapor Pressure: 2.46E-14mmHg at 25°C
• Boiling Point: 599.6°Cat760mmHg
• Flash Point: 316.4°C
• Density: 1.357g/cm³
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 7
• Exact Mass: 369.13247072
• Heavy Atom Count: 27
• Complexity: 556

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC2=C(C(=C1)[N+](=O)[O-])C(=O)N(C2=O)CCCCCOC3=CC=C(C=C3)N

Technology Process of Phthalimide, N-(5-(p-aminophenoxy)pentyl)-3-nitro-

There total 4 articles about Phthalimide, N-(5-(p-aminophenoxy)pentyl)-3-nitro- 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:

N-[5-(4-acetylamino-phenoxy)-pentyl]-phthalimide (113057-76-4) → 2-[5-(4-amino-phenoxy)-pentyl]-4-nitro-isoindoline-1,3-dione (108368-14-5)

Guidance literature:

Multi-step reaction with 3 steps

1: N₂H₄

2: 180 - 190 °C

3: Hydrolysis

With hydrazine;

Reference yield:

2-[5-(4-acetylamino-phenoxy)-pentyl]-4-nitro-isoindoline-1,3-dione (102659-73-4) → 2-[5-(4-amino-phenoxy)-pentyl]-4-nitro-isoindoline-1,3-dione (108368-14-5)

Guidance literature:

Hydrolysis;

Reference yield:

3-nitrophthalic acid anhydride (641-70-3) → 2-[5-(4-amino-phenoxy)-pentyl]-4-nitro-isoindoline-1,3-dione (108368-14-5)

Guidance literature:

Multi-step reaction with 2 steps

1: 180 - 190 °C

2: Hydrolysis

upstream raw materials:

2-[5-(4-acetylamino-phenoxy)-pentyl]-4-nitro-isoindoline-1,3-dione

3-nitrophthalic acid anhydride

acetic acid-[4-(5-amino-pentyloxy)-anilide]

N-[5-(4-acetylamino-phenoxy)-pentyl]-phthalimide

Downstream raw materials:

4-amino-2-[5-(4-amino-phenoxy)-pentyl]-isoindoline-1,3-dione