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2-Aminoadamantane

Basic Information

  • CAS No.:13074-39-0
  • Purity:99%
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Details

Factory Sells Best Quality 2-Aminoadamantane 13074-39-0 with GMP standards

  • Molecular Formula:C10H17N
  • Molecular Weight:151.252
  • Boiling Point:226.1 °C at 760 mmHg 
  • Flash Point:96.5 °C 
  • PSA：26.02000 
  • Density:1.028 g/cm3 
  • LogP:2.47010 

2-Aminoadamantane(Cas 13074-39-0) Usage

General Description

2-Aminoadamantane is a chemical compound with the molecular formula C10H17N. It is a derivative of adamantane and is classified as an aminoadamantane. 2-Aminoadamantane is used as a reagent in the synthesis of various pharmaceuticals and is known to have psychoactive effects on the central nervous system. It has been studied for its potential use in the treatment of Parkinson's disease, attention deficit hyperactivity disorder, and depression. Additionally, 2-Aminoadamantane has also been researched for its antiviral properties and its potential to inhibit the replication of certain viruses. Overall, 2-Aminoadamantane is a versatile chemical compound with various potential applications in the fields of medicine and virology.

InChI:InChI=1/C10H17N/c11-10-8-2-6-1-7(4-8)5-9(10)3-6/h6-10H,1-5,11H2

13074-39-0 Relevant articles

Photoinduced hydrogen atom abstraction in N-(adamantyl)phthalimides: structure-reactivity study in the solid state

Basari?, Nikola,Horvat, Margareta,Frankovi?, Oliver,Mlinari?-Majerski, Kata,Neud?rfl, J?rg,Griesbeck, Axel G.

, p. 1438 - 1443 (2009)

Adamantyl-functionalized phthalimides we...

A Facile Reduction of Azides to Amines Using Hydrazine

Malik, A. A.,Preston, S. B.,Archibald, T. G.,Cohen, M. P.,Baum, K.

, p. 450 - 451 (1989)

A variety of alkyl and aryl azides were ...

New one-step synthesis of isonitriles

Bardsley, Kathryn,Hagigeorgiou, Michael,Lengyel, Istvan,Cesare, Victor

, p. 1727 - 1733 (2013)

A new one-step synthesis of isonitriles ...

General and selective synthesis of primary amines using Ni-based homogeneous catalysts

Beller, Matthias,Chandrashekhar, Vishwas G.,Jagadeesh, Rajenahally V.,Jiao, Haijun,Murugesan, Kathiravan,Wei, Zhihong

, p. 4332 - 4339 (2020/05/18)

The development of base metal catalysts ...

The Synthesis of Primary Amines through Reductive Amination Employing an Iron Catalyst

B?umler, Christoph,Bauer, Christof,Kempe, Rhett

, p. 3110 - 3114 (2020/06/01)

The reductive amination of ketones and a...

Cerium-Catalyzed C-H Functionalizations of Alkanes Utilizing Alcohols as Hydrogen Atom Transfer Agents

An, Qing,Chen, Yuegang,Liu, Weimin,Pan, Hui,Wang, Xin,Wang, Ziyu,Zhang, Kaining,Zuo, Zhiwei

supporting information, p. 6216 - 6226 (2020/04/27)

Modern photoredox catalysis has traditio...

Reusable Nickel Nanoparticles-Catalyzed Reductive Amination for Selective Synthesis of Primary Amines

Murugesan, Kathiravan,Beller, Matthias,Jagadeesh, Rajenahally V.

supporting information, p. 5064 - 5068 (2019/03/19)

The preparation of nickel nanoparticles ...

13074-39-0 Process route

2-adamantanone oxime
4500-12-3

2-adamantanone oxime

1-adamantanol
700-57-2

1-adamantanol

N-(2-adamantyl)amine
13074-39-0

N-(2-adamantyl)amine

Conditions
Conditions Yield
With NiAl2; potassium hydroxide; In tetrahydrofuran; water; Reflux;
2-Adamantanone
700-58-3

2-Adamantanone

1-adamantanol
700-57-2

1-adamantanol

N-(2-adamantyl)amine
13074-39-0

N-(2-adamantyl)amine

Conditions
Conditions Yield
With platinum-doped magnesium oxide; ammonia; hydrogen; In o-xylene; at 100 ℃; for 20h; Autoclave;
45 %Chromat.
43 %Chromat.
With CeO2#dotPt; ammonia; hydrogen; In o-xylene; at 100 ℃; for 20h; Autoclave;
58 %Chromat.
16 %Chromat.
Multi-step reaction with 2 steps
1: hydroxylamine hydrochloride; sodium hydroxide / ethanol; water / 20 °C
2: potassium hydroxide; NiAl2 / water; tetrahydrofuran / Reflux
With hydroxylamine hydrochloride; NiAl2; potassium hydroxide; sodium hydroxide; In tetrahydrofuran; ethanol; water;

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