N-benzyladamantan-2-amine

Base Information

• Chemical Name: N-benzyladamantan-2-amine
• CAS No.: 39234-37-2
• Molecular Weight: 241.376
• Hs Code.: 2921499090
• DSSTox Substance ID: DTXSID70960006
• Nikkaji Number: J395.466H
• Wikidata: Q82941001
• Mol file: 39234-37-2.mol

Synonyms:2-(N-benzylamino)adamantane;bemantane;bemantane hydrochloride

Chemical Property of N-benzyladamantan-2-amine

Chemical Property:

• Vapor Pressure: 2.48E-05mmHg at 25°C
• Boiling Point: 358.8°Cat760mmHg
• Flash Point: 177.5°C
• PSA: 12.03000
• Density: g/cm³
• LogP: 3.99180
• XLogP3: 3.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 241.183049738
• Heavy Atom Count: 18
• Complexity: 264

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C2CC3CC1CC(C2)C3NCC4=CC=CC=C4

Technology Process of N-benzyladamantan-2-amine

There total 8 articles about N-benzyladamantan-2-amine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

C44H41Cl8Cu2N5 + toluene (108-88-3,15644-74-3,16713-13-6) → N-benzyl-1-aminoadamantane (39234-37-2)

Guidance literature:

In benzene; at 80 ℃; for 3h; Inert atmosphere;

DOI:10.1002/anie.200804304

Reference yield: 100.0%

→ N-benzyl-1-aminoadamantane (39234-37-2)

Guidance literature:

With acetic acid; In methanol; at 20 ℃; for 48h;

Reference yield: 31.0%

1-azidoadamantane (34197-88-1) + toluene (108-88-3,15644-74-3,16713-13-6) → N-benzyl-1-aminoadamantane (39234-37-2)

Guidance literature:

With [(copper)CH(C(CH3)NC6H3Cl2)2]2(μ-benzene); In benzene; at 110 ℃; for 4h; Inert atmosphere;

DOI:10.1002/anie.200804304

upstream raw materials:

toluene

Isopropylbenzene

ethylbenzene

1-azidoadamantane

Downstream raw materials:

N-(2-adamantyl)amine

N-(2-adamantyl)benzylideneamine