4-Nitro-2,6-diphenylphenol

Base Information

• Chemical Name: 4-Nitro-2,6-diphenylphenol
• CAS No.: 2423-73-6
• Molecular Formula: C18H13 N O3
• Molecular Weight: 291.306
• Hs Code.: 2906299090
• European Community (EC) Number: 621-922-5
• DSSTox Substance ID: DTXSID40347800
• Nikkaji Number: J2.639.346I
• Wikidata: Q82122047
• Mol file: 2423-73-6.mol

Synonyms:4-Nitro-2,6-diphenylphenol;2423-73-6;5'-Nitro-[1,1':3',1''-terphenyl]-2'-ol;Phenol, 2,6-diphenyl-4-nitro-;4-nitro-2,6-diphenyl-phenol;SCHEMBL2437022;DTXSID40347800;2'-Hydroxy-5'-nitro-m-terphenyl;CAA42373;4-Nitro-2,6-diphenylphenol, 99%;MFCD00075055;AKOS005216534;AKOS015912604;AS-63642;CS-0318267;FT-0634261;N0674;5'-nitro-[1,1';3'1'']terphenyl-2'-ol;3',1'']terphenyl-2'-ol;T72137;A817158;5-NITRO-3-PHENYL-[1,1'-BIPHENYL]-2-OL;J-015407;1,6,7,12-Tetra-tert-butylphenoxyperylene-3,4,9,10-tetracarboxylicdianhydride

Chemical Property of 4-Nitro-2,6-diphenylphenol

Chemical Property:

• Vapor Pressure: 6.65E-09mmHg at 25°C
• Melting Point: 137-139 °C(lit.)
• Refractive Index: 1.648
• Boiling Point: 455.2°C at 760 mmHg
• PKA: 7.10±0.44(Predicted)
• Flash Point: 187.1°C
• PSA: 66.05000
• Density: 1.265g/cm³
• LogP: 5.15760
• Water Solubility.: Insoluble in water
• XLogP3: 4.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 291.08954328
• Heavy Atom Count: 22
• Complexity: 341

Purity/Quality:

97% ^*data from raw suppliers

4-Nitro-2,6-diphenylphenol >98.0%(T) ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CC(=CC(=C2O)C3=CC=CC=C3)[N+](=O)[O-]

Technology Process of 4-Nitro-2,6-diphenylphenol

There total 1 articles about 4-Nitro-2,6-diphenylphenol 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:

C40H51NO (1207510-94-8) + C70H67N9O12 → 2,6-diphenyl-4-nitrophenol (2423-73-6) + C92H105N9O10

Guidance literature:

With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 40 ℃; for 48h;

DOI:10.1039/d0sc05369d

Reference yield: 85.0%

2,6-diphenyl-4-nitrophenol (2423-73-6) → 2,6-diphenyl-p-aminophenol (50432-01-4)

Guidance literature:

With sodium dithionite; In sodium hydroxide; for 0.25h; Heating;

DOI:10.1055/s-1988-27662

Reference yield: 72.0%

2,6-diphenyl-4-nitrophenol (2423-73-6) → 2-nitro-4-phenyldibenzofuran (1357581-63-5)

Guidance literature:

With copper diacetate; caesium carbonate; Trimethylacetic acid; In dimethyl sulfoxide; at 140 ℃; for 48h; air;

DOI:10.1021/ol203442a

upstream raw materials:

C₄₀H₅₁NO

Downstream raw materials:

2,6-diphenyl-p-aminophenol

betaine 30

Bis<4-(2,4,6-triphenyl-1-pyridinio)-2,6-diphenylphenyl>disulfanbis(tetrafluoroborat)

Bis<(4-amino-2,6-diphenyl)phenyl>disulfan