2,3-Diphenylbenzo[f]quinoxaline

Base Information

• Chemical Name: 2,3-Diphenylbenzo[f]quinoxaline
• CAS No.: 10322-25-5
• Molecular Formula: C₂₄H₁₆N₂
• Molecular Weight: 332.404
• European Community (EC) Number: 654-687-2
• NSC Number: 163177
• DSSTox Substance ID: DTXSID80303884
• Wikidata: Q82049377
• Mol file: 10322-25-5.mol

Synonyms:2,3-diphenylbenzo[f]quinoxaline;10322-25-5;2,3-diphenyl-5,6-benzoquinoxaline;NSC163177;2,3-diphenylbenzoquinoxaline;BIDD:GT0246;SCHEMBL15818339;DTXSID80303884;AKOS024332223;NSC-163177;FT-0753482

Chemical Property of 2,3-Diphenylbenzo[f]quinoxaline

Chemical Property:

• Vapor Pressure: 1.31E-09mmHg at 25°C
• Boiling Point: 499.2oC at 760 mmHg
• Flash Point: 217.1oC
• PSA: 25.78000
• Density: 1.21g/cm3
• LogP: 6.11700
• XLogP3: 5.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 332.131348519
• Heavy Atom Count: 26
• Complexity: 451

Purity/Quality:

2,3-Diphenyl-5,6-benzoquinoxaline ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=NC3=C(C4=CC=CC=C4C=C3)N=C2C5=CC=CC=C5

Technology Process of 2,3-Diphenylbenzo[f]quinoxaline

There total 5 articles about 2,3-Diphenylbenzo[f]quinoxaline 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:

→ 2,3-diphenyl-benzo[f]quinoxaline (10322-25-5)

Guidance literature:

With ethanol; iron(III) chloride;

Reference yield:

1-nitro-2-naphthylamine (606-57-5) → 2,3-diphenyl-benzo[f]quinoxaline (10322-25-5)

Guidance literature:

Multi-step reaction with 2 steps

1: aqueous alcohol; tin dichloride

2: alcohol

With ethanol; tin(ll) chloride;

Reference yield:

benzil (134-81-6) + 1,2-diaminonaphthalene (938-25-0) → 2,3-diphenyl-benzo[f]quinoxaline (10322-25-5)

Guidance literature:

With ethanol;

upstream raw materials:

benzil

1,2-diaminonaphthalene

phenyl benzyl ketone

1-phenylazo-2-naphthylamine

Downstream raw materials:

2,3-diphenyl-benzo[f]quinoxaline-5,6-dione

3-(2-carboxy-phenyl)-5,6-diphenyl-pyrazine-2-carboxylic acid