Ethanone, 1-[4-[(4-hydroxy-1-naphthalenyl)azo]phenyl]-

Base Information

• Chemical Name: Ethanone, 1-[4-[(4-hydroxy-1-naphthalenyl)azo]phenyl]-
• CAS No.: 27959-62-2
• Molecular Formula: C₁₈H₁₄N₂O₂
• Molecular Weight: 290.321
• DSSTox Substance ID: DTXSID40425435
• Nikkaji Number: J2.263.672C
• Mol file: 27959-62-2.mol

Synonyms:Ethanone, 1-[4-[(4-hydroxy-1-naphthalenyl)azo]phenyl]-;27959-62-2;DTXSID40425435;4-(4-Acetylphenylazo)-1-naphthol;AKOS003416769

Chemical Property of Ethanone, 1-[4-[(4-hydroxy-1-naphthalenyl)azo]phenyl]-

Chemical Property:

• XLogP3: 4.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 290.105527694
• Heavy Atom Count: 22
• Complexity: 415

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=O)C1=CC=C(C=C1)N=NC2=CC=C(C3=CC=CC=C32)O

Technology Process of Ethanone, 1-[4-[(4-hydroxy-1-naphthalenyl)azo]phenyl]-

There total 5 articles about Ethanone, 1-[4-[(4-hydroxy-1-naphthalenyl)azo]phenyl]- 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:

α-naphthol (90-15-3) + C8H7ClN2O → 4-hydroxynaphthylazo-4'-acetylbenzene (27959-62-2)

Guidance literature:

With sodium hydroxide; at 0 - 5 ℃;

DOI:10.1080/15421406.2012.703029

Reference yield:

α-naphthol (90-15-3) + 4'-dimethylaminoacetophenone (2124-31-4) → 4-hydroxynaphthylazo-4'-acetylbenzene (27959-62-2)

Guidance literature:

With hydrogenchloride; isopentyl nitrite; Yield given. Multistep reaction; 1.) ethanol;

DOI:10.1016/S0022-328X(00)86094-5

Reference yield:

p-aminobenzophenone (99-92-3) → 4-hydroxynaphthylazo-4'-acetylbenzene (27959-62-2)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogenchloride; sodium nitrite / 0 - 5 °C

2: sodium hydroxide / 0 - 5 °C

With hydrogenchloride; sodium hydroxide; sodium nitrite;

DOI:10.1080/15421406.2012.703029

upstream raw materials:

α-naphthol

4-Acetyl-phenyl-diazonium

4'-dimethylaminoacetophenone

p-aminobenzophenone