2-Naphthylhydrazine hydrochloride

  • CAS:2243-58-5
  • purity:99%
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Details

Chemical plants supply high-quality 2-Naphthylhydrazine hydrochloride 2243-58-5 in bulk

  • Molecular Formula:C10H10N2.HCl
  • Molecular Weight:194.664
  • Vapor Pressure:1.87E-05mmHg at 25°C 
  • Melting Point:123 °C 
  • Boiling Point:362.9 °C at 760 mmHg 
  • Flash Point:203.9 °C 
  • PSA:38.05000 
  • Density:1.215g/cm3 
  • LogP:3.70070 

2-Naphthylhydrazine hydrochloride(Cas 2243-58-5) Usage

InChI:InChI=1/C10H10N2.ClH/c11-12-10-6-5-8-3-1-2-4-9(8)7-10;/h1-7,12H,11H2;1H

2243-58-5 Relevant articles

Discovery of Pyrazolocarboxamides as Potent and Selective Receptor Interacting Protein 2 (RIP2) Kinase Inhibitors

Haffner, Curt D.,Charnley, Adam K.,Aquino, Christopher J.,Casillas, Linda,Convery, Máire A.,Cox, Julie A.,Elban, Mark A.,Goodwin, Nicole C.,Gough, Peter J.,Haile, Pamela A.,Hughes, Terry V.,Knapp-Reed, Beth,Kreatsoulas, Constantine,Lakdawala, Ami S.,Li, Huijie,Lian, Yiqian,Lipshutz, David,Mehlmann, John F.,Ouellette, Michael,Romano, Joseph,Shewchuk, Lisa,Shu, Arthur,Votta, Bartholomew J.,Zhou, Huiqiang,Bertin, John,Marquis, Robert W.

supporting information, p. 1518 - 1523 (2019/10/19)

Herein we report the discovery of pyrazo...

A 10 - bromo - 7H - benzo [c] carbazole preparation method (by machine translation)

-

Paragraph 0091; 0095, (2019/10/17)

The invention discloses a 10 - bromo - 7...

Synthesis of Aryl Hydrazines via CuI/BMPO Catalyzed Cross-Coupling of Aryl Halides with Hydrazine Hydrate in Water

Kumar, Siripuram Vijay,Ma, Dawei

supporting information, p. 1003 - 1006 (2018/09/20)

The N,N’-bis(2,6-dimethylphenyl)oxalamid...

Asymmetric catalysis on the nanoscale: The organocatalytic approach to helicenes

Koetzner, Lisa,Webber, Matthew J.,Martinez, Alberto,Defusco, Claudia,List, Benjamin

supporting information, p. 5202 - 5205 (2014/05/20)

The first asymmetric organocatalytic syn...

2243-58-5 Process route

naphthalen-2-ylamine
91-59-8

naphthalen-2-ylamine

2-naphthylhydrazine hydrochloride
2243-58-5

2-naphthylhydrazine hydrochloride

Conditions
Conditions Yield
naphthalen-2-ylamine; With hydrogenchloride; sodium nitrite; In water; for 1h; Cooling with ice;
With tin(ll) chloride; In water; for 3.5h; Cooling with ice;
63%
With hydrogenchloride; tin(ll) chloride; sodium nitrite; Multistep reaction; 1.) -5 deg C to 0 deg C, 0.75 h, 2.) 1 h;
naphthalen-2-ylamine; With hydrogenchloride; sodium nitrite; In water; at 0 ℃; for 0.416667h;
With hydrogenchloride; tin(ll) chloride; In water; at 0 ℃; for 0.5h;
naphthalen-2-ylamine; With hydrogenchloride; sodium nitrite; In water; at -5 - 0 ℃; for 0.5h;
With tin(ll) chloride; In water; at 0 - 20 ℃;
2-bromonaphthalene
580-13-2

2-bromonaphthalene

2-naphthylhydrazine hydrochloride
2243-58-5

2-naphthylhydrazine hydrochloride

Conditions
Conditions Yield
2-bromonaphthalene; With potassium phosphate; copper(l) iodide; N,N′-bis(2,6-dimethylphenyl)oxalamide; cetyltrimethylammonim bromide; In water; at 80 ℃; for 0.25h; Schlenk technique; Inert atmosphere; Sealed tube;
With hydrazine hydrate; In water; at 80 ℃; Inert atmosphere; Schlenk technique; Sealed tube;
With hydrogenchloride; In water; pH=3 - 4; Inert atmosphere; Schlenk technique; Sealed tube;
70%
Multi-step reaction with 2 steps
1.1: s-BuLi / tetrahydrofuran; cyclohexane / 0.5 h / -78 °C
1.2: tetrahydrofuran; cyclohexane / -78 - 20 °C
2.1: HCl / dioxane; propan-2-ol / 0.5 h / 60 °C
With hydrogenchloride; sec.-butyllithium; In tetrahydrofuran; 1,4-dioxane; cyclohexane; isopropyl alcohol;

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