1,1'-(3-Nitrobenzylidene)DI(2-naphthol)

Base Information

• Chemical Name: 1,1'-(3-Nitrobenzylidene)DI(2-naphthol)
• CAS No.: 34504-00-2
• Molecular Formula: C27H19NO4
• Molecular Weight: 421.452
• European Community (EC) Number: 666-120-6
• Mol file: 34504-00-2.mol

Synonyms:1,1'-(3-NITROBENZYLIDENE)DI(2-NAPHTHOL);SCHEMBL11536669;1-[(2-hydroxynaphthalen-1-yl)(3-nitrophenyl)methyl]naphthalen-2-ol;AKOS024431559;34504-00-2;1,1'-((3-Nitrophenyl)methylene)bis(naphthalen-2-ol)

Chemical Property of 1,1'-(3-Nitrobenzylidene)DI(2-naphthol)

Chemical Property:

• XLogP3: 6.9
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 421.13140809
• Heavy Atom Count: 32
• Complexity: 612

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C=CC(=C2C(C3=CC(=CC=C3)[N+](=O)[O-])C4=C(C=CC5=CC=CC=C54)O)O

Technology Process of 1,1'-(3-Nitrobenzylidene)DI(2-naphthol)

There total 7 articles about 1,1'-(3-Nitrobenzylidene)DI(2-naphthol) 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: 97.0%

3-nitro-benzaldehyde (99-61-6) + β-naphthol (135-19-3) → 1,1'-((3-nitrophenyl)methylene)bis(naphthalen-2-ol) (34504-00-2)

Guidance literature:

With molybdophosphoric acid hydrate; In dichloromethane; at 40 ℃; for 1h;

DOI:10.1007/BF03246020

Reference yield: 20.0%

3-nitro-benzaldehyde (99-61-6) + aniline (62-53-3) + β-naphthol (135-19-3) → (3-nitrobenzylidene)aniline (5676-82-4) + 1,1'-((3-nitrophenyl)methylene)bis(naphthalen-2-ol) (34504-00-2)

Guidance literature:

With sodium hydroxide; In water; at 90 ℃; for 8h;

DOI:10.1039/c6ra28599f

Reference yield:

3-nitro-benzaldehyde (99-61-6) → 1,1'-((3-nitrophenyl)methylene)bis(naphthalen-2-ol) (34504-00-2)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; kaolin / neat (no solvent) / 0.02 h / 125 °C

1.2: 255 / 125 °C

2.1: neat (no solvent) / 125 °C

With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; kaolin; In neat (no solvent);

DOI:10.1016/j.cclet.2012.08.008

upstream raw materials:

3-nitro-benzaldehyde

β-naphthol

[3-Nitro-dl-α-(2-oxy-naphthyl-(1))-benzyl]-anilin

aniline

Downstream raw materials:

C₂₇H₁₇NO₄

(1RS,1'RS)-1'-(3-nitro-phenyl)-1'H-spiro[naphthalene-1,2'-naphtho[2,1-b]furan]-2-one

14-(3-nitrophenyl)-14H-dibenzo[a,j]xanthene

β-naphthol