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2,2'-DIBROMO-1,1'-BINAPHTHYL

  • Product Name 2,2'-DIBROMO-1,1'-BINAPHTHYL
  • cas 74866-28-7
  • purity 99%
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Quality manufacturer supply 2,2'-DIBROMO-1,1'-BINAPHTHYL 74866-28-7 in stock with high standard

  • Molecular Formula: C20H12Br2
  • Molecular Weight: 412.123
  • Melting Point: 178-183 °C 
  • Boiling Point: 464.1 °C at 760 mmHg 
  • Flash Point: 273.6 °C 
  • PSA: 0.00000 
  • Density: 1.614 g/cm3 
  • LogP: 7.18500 

74866-28-7 Relevant articles

Synthesis method of 2, 2 '-bisdiphenylphosphino-1, 1'-binaphthalene

-

, (2020/09/12)

The invention relates to a synthesis met...

Mixed er-NHC/phosphine Pd(ii) complexes and their catalytic activity in the Buchwald-Hartwig reaction under solvent-free conditions

Ageshina, Alexandra A.,Sterligov, Grigorii K.,Rzhevskiy, Sergey A.,Topchiy, Maxim A.,Chesnokov, Gleb A.,Gribanov, Pavel S.,Nechaev, Mikhail S.,Asachenko, Andrey F.,Bermeshev, Maxim V.,Melnikova, Elizaveta K.

supporting information, p. 3447 - 3452 (2019/04/30)

A series of novel (NHC)PdCl2-PR3 complex...

Reconnaissance of reactivity of an Ag(II)SO4 one-electron oxidizer towards naphthalene derivatives

Budniak, Adam K.,Masny, Micha?,Prezelj, Kristina,Grzeszkiewicz, Miko?aj,Gawraczyński, Jakub,Dobrzycki, ?ukasz,Cyrański, Micha? K.,Ko?miński, Wiktor,Mazej, Zoran,Fija?kowski, Karol J.,Grochala, Wojciech,Leszczyński, Piotr J.

supporting information, p. 10742 - 10749 (2017/10/03)

We test divalent silver sulphate, Ag(ii)...

Highly sterically hindered binaphthalene-based monophosphane ligands: Synthesis and application in stereoselective Suzuki-Miyaura reactions

Meskova, Michaela,Putala, Martin

, p. 894 - 902 (2013/09/23)

A series of new sterically hindered (R)-...

74866-28-7 Process route

1,1'-binaphthalene-2,2'-diamine
4488-22-6,18531-95-8

1,1'-binaphthalene-2,2'-diamine

2,2'-dibromo-1,1'-binaphthyl
74866-28-7,86688-08-6,150024-49-0

2,2'-dibromo-1,1'-binaphthyl

Conditions
Conditions Yield
1,1'-binaphthalene-2,2'-diamine; With hydrogen bromide; In water; at 20 ℃; Large scale;
With sodium nitrite; In water; at -5 ℃; for 0.5h; Large scale;
With hydrogen bromide; copper(I) bromide; In water; at 70 ℃; for 2.5h; Large scale;
94%
1,1'-bi-2-naphthol
602-09-5

1,1'-bi-2-naphthol

2,2'-dibromo-1,1'-binaphthyl
74866-28-7,86688-08-6,150024-49-0

2,2'-dibromo-1,1'-binaphthyl

Conditions
Conditions Yield
With triphenylphosphine dibromide 1:1 addition complex; at 320 ℃;
45%
With triphenylphosphine dibromide 1:1 addition complex; at 320 ℃;
45%
1,1'-bi-2-naphthol; With bromine; triphenylphosphine; In acetonitrile; at 60 ℃; for 0.5h;
at 240 - 320 ℃; for 2.5h;
45%
With bromine; triphenylphosphine; In acetonitrile; at 320 ℃;
39%
1,1'-bi-2-naphthol; With bromine; triphenylphosphine; In acetonitrile; at 60 ℃; for 0.5h;
In melt; at 260 - 320 ℃; for 2.5h;
21%
Multi-step reaction with 2 steps
1.1: ammonia; sodium hydrogencarbonate / water / 150 °C / Large scale
2.1: hydrogen bromide / water / 20 °C / Large scale
2.2: 0.5 h / -5 °C / Large scale
2.3: 2.5 h / 70 °C / Large scale
With ammonia; hydrogen bromide; sodium hydrogencarbonate; In water; 1.1: |Bucherer Carbazole Synthesis / 2.1: |Sandmeyer Reaction;

74866-28-7 Upstream products

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    602-09-5

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74866-28-7 Downstream products

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    100165-87-5

    2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl dioxide

  • 139139-84-7
    139139-84-7

    (+/-)-2,2'-bis(dicyclohexylphosphinyl)-1,1'-binaphthyl

  • 139139-84-7
    139139-84-7

    (R)-(-)-2,2'-bis(dicyclohexylphosphinoyl)-1,1'-binaphthyl

  • 139139-84-7
    139139-84-7

    (S)-(+)-2,2'-bis(dicyclohexylphosphinoyl)-1,1'-binaphthyl

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