1,1'-Azonaphthalene

  • CAS：487-10-5
  • purity：99%
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Details

Quality manufacturer supply 1,1'-Azonaphthalene 487-10-5 in stock with high standard

  • Molecular Formula: C20H14 N2
  • Molecular Weight: 282.345
  • Vapor Pressure: 4.51E-09mmHg at 25°C 
  • Melting Point: 190°C 
  • Refractive Index: 1.6450 (estimate) 
  • Boiling Point: 484.5°Cat760mmHg 
  • Flash Point: 239.8°C 
  • PSA： 24.72000 
  • Density: 1.12g/cm3 
  • LogP: 6.40840 

1,1'-Azonaphthalene(Cas 487-10-5) Usage

Safety Profile

Questionable carcinogen withexperimental tumorigenic data. When heated todecomposition it emits toxic fumes of NOx.

InChI:InChI=1/C20H14N2/c1-3-11-17-15(7-1)9-5-13-19(17)21-22-20-14-6-10-16-8-2-4-12-18(16)20/h1-14H/b22-21+

487-10-5 Relevant articles

Tandem selective reduction of nitroarenes catalyzed by palladium nanoclusters

Yan, Ziqiang,Xie, Xiaoyu,Song, Qun,Ma, Fulei,Sui, Xinyu,Huo, Ziyu,Ma, Mingming

supporting information, p. 1301 - 1307 (2020/03/11)

We report a catalytic tandem reduction o...

Immobilized antimony species on magnetite: A novel and highly efficient magnetically reusable nanocatalyst for direct and gram-scale reductive-coupling of nitroarenes to azoarenes

Zeynizadeh, Behzad,Faraji, Fariba

, p. 13112 - 13121 (2019/05/10)

In this study, magnetic nanoparticles of...

Aromatic amine oxidation process for preparing aromatic azobenzene method

-

Paragraph 0013; 0017, (2017/10/11)

The invention relates to a method for pr...

Mesoporous manganese oxide catalyzed aerobic oxidative coupling of anilines to aromatic azo compounds

Dutta, Biswanath,Biswas, Sourav,Sharma, Vinit,Savage, Nancy Ortins,Alpay, S. Pamir,Suib, Steven L.

supporting information, p. 2171 - 2175 (2016/02/18)

Herein we introduce an environmentally f...

487-10-5 Process route

1-azidonaphthalene
6921-40-0

1-azidonaphthalene

dibenzo[a,h]phenazine
226-47-1

dibenzo[a,h]phenazine

1-amino-naphthalene
134-32-7

1-amino-naphthalene

1,2-di(naphthalen-1-yl)diazene
487-10-5

1,2-di(naphthalen-1-yl)diazene

Conditions
Conditions Yield
In various solvent(s); at 155 ℃; for 12h;
20%
10%
12%
1-azidonaphthalene
6921-40-0

1-azidonaphthalene

1-amino-naphthalene
134-32-7

1-amino-naphthalene

1,2-di(naphthalen-1-yl)diazene
487-10-5

1,2-di(naphthalen-1-yl)diazene

Conditions
Conditions Yield
In diethylamine; Mechanism; Kinetics; Irradiation; different irradiation methods;
50 % Chromat.
4 % Chromat.

487-10-5 Upstream products

  • 60-29-7
    60-29-7

    diethyl ether

  • 86-57-7
    86-57-7

    1-Nitronaphthalene

  • 925-90-6
    925-90-6

    ethylmagnesium bromide

  • 64-17-5
    64-17-5

    ethanol

487-10-5 Downstream products

  • 481-91-4
    481-91-4

    4,4'-diamino-1,1'-binaphthyl

  • 134-32-7
    134-32-7

    1-amino-naphthalene

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