5,6,7,8-Tetrahydro-1-naphthylamine

  • Name: 5,6,7,8-Tetrahydro-1-naphthylamine
  • CAS: 2217-41-6
  • Purity: 99%
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Details

Reputable factory supply 5,6,7,8-Tetrahydro-1-naphthylamine 2217-41-6 in stock with high standard

  • Molecular Formula: C10H13N
  • Molecular Weight: 147.22
  • Appearance/Colour: Clear yellow to brown liquid 
  • Vapor Pressure: 0.0032mmHg at 25°C 
  • Melting Point: 38 °C(lit.) 
  • Refractive Index: n20/D 1.590(lit.)  
  • Boiling Point: 283.2 °C at 760 mmHg 
  • PKA: 4.56±0.20(Predicted) 
  • Flash Point: 136.4 °C 
  • PSA： 26.02000 
  • Density: 1,062 g/cm3 
  • LogP: 2.72880 

5,6,7,8-Tetrahydro-1-naphthylamine(Cas 2217-41-6) Usage

InChI:InChI=1/C10H13N/c11-10-7-3-5-8-4-1-2-6-9(8)10/h3,5,7H,1-2,4,6,11H2

2217-41-6 Relevant articles

-

Shagalov et al.

, (1978)

-

-

Gal'bershtam,M.A. et al.

, (1977)

-

Ether compound and pharmaceutical application thereof in prevention and treatment of diabetes and metabolic syndrome

-

Paragraph 0260-0261; 0487-0486, (2021/07/24)

The invention relates to an ether compou...

C-H Amination of Arenes with Hydroxylamine

See, Yi Yang,Sanford, Melanie S.

supporting information, p. 2931 - 2934 (2020/04/09)

This Letter describes the development of...

Cobalt-Nanoparticles Catalyzed Efficient and Selective Hydrogenation of Aromatic Hydrocarbons

Murugesan, Kathiravan,Senthamarai, Thirusangumurugan,Alshammari, Ahmad S.,Altamimi, Rashid M.,Kreyenschulte, Carsten,Pohl, Marga-Martina,Lund, Henrik,Jagadeesh, Rajenahally V.,Beller, Matthias

, p. 8581 - 8591 (2019/09/12)

The development of inexpensive and pract...

Regioselective and Chemoselective Reduction of Naphthols Using Hydrosilane in Methanol: Synthesis of the 5,6,7,8-Tetrahydronaphthol Core

He, Yuan,Tang, Jinghua,Luo, Meiming,Zeng, Xiaoming

supporting information, p. 4159 - 4163 (2018/07/29)

A regioselective and chemoselective meth...

2217-41-6 Process route

1-amino-naphthalene
134-32-7

1-amino-naphthalene

1,2,3,4-tetrahydronaphthalen-1-amine
2217-40-5

1,2,3,4-tetrahydronaphthalen-1-amine

1-amino-5,6,7,8-tetrahydronaphthalene
2217-41-6

1-amino-5,6,7,8-tetrahydronaphthalene

Conditions
Conditions Yield
With hydrogen; In tetrahydrofuran; at 99.99 ℃; for 5h; under 11251.1 Torr; chemoselective reaction; Autoclave; Green chemistry;
1-amino-naphthalene
134-32-7

1-amino-naphthalene

1-amino-5,6,7,8-tetrahydronaphthalene
2217-41-6

1-amino-5,6,7,8-tetrahydronaphthalene

Conditions
Conditions Yield
With hydrogen; In ethanol; at 25 - 30 ℃;
94.6%
With cobalt(II) chloride hexahydrate; lithium; In tetrahydrofuran; at 66 ℃; for 6h; regioselective reaction; Inert atmosphere;
90%
With hydrogen; In water; tert-butyl alcohol; at 135 ℃; for 24h; Autoclave;
85%
With chloro(1,5-cyclooctadiene)rhodium(I) dimer; In methanol; at 40 ℃; for 12h; regioselective reaction; Inert atmosphere;
55%
With pentan-1-ol; sodium;
With ethanol; nickel; at 150 ℃; under 110326 Torr; Hydrogenation;
With lithium; ethylamine;
With ethanol; sodium; at 130 ℃;
With methanol; sodium; at 130 - 140 ℃;
Multi-step reaction with 2 steps
1: Li, liq. NH3
2: H2 / Pd-C / 2280 Torr
With ammonia; hydrogen; lithium; palladium on activated charcoal;
With hydrogen; In tetrahydrofuran; at 30 ℃; for 16h; under 15001.5 Torr; chemoselective reaction; Inert atmosphere; Schlenk technique; Autoclave; Glovebox;
With water; sodium;

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