1-Adamantyl(4-nitrobenzyl)amine

Base Information

Chemical Name:1-Adamantyl(4-nitrobenzyl)amine
CAS No.:206053-11-4
Molecular Formula:C17H22N2O2
Molecular Weight:286.374
Hs Code.:2921499090
DSSTox Substance ID:DTXSID70386065
Nikkaji Number:J3.359.688J
Wikidata:Q82179223
ChEMBL ID:CHEMBL2324188

Synonyms:206053-11-4;1-ADAMANTYL(4-NITROBENZYL)AMINE;N-[(4-nitrophenyl)methyl]adamantan-1-amine;CHEMBRDG-BB 5554037;N-(4-Nitrobenzyl)adamantan-1-amine;Adamantan-1-yl-(4-nitro-benzyl)-amine;Oprea1_291557;Oprea1_406085;SCHEMBL3360529;CHEMBL2324188;DTXSID70386065;N-(4-nitrobenzyl)tricyclo[3.3.1.1~3,7~]decan-1-amine;XGZKNPFIGODKCG-UHFFFAOYSA-N;N-(p-Nitrobenzyl)adamantane-1-amine;STK145860;AKOS000251639;N-[(4-Nitrophenyl)methyl]tricyclo[3.3.1.1~3,7~]decan-1-amine

Suppliers and Price of 1-Adamantyl(4-nitrobenzyl)amine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
1-ADAMANTYL(4-NITROBENZYL)AMINE 95.00%
5MG
$ 500.14

Total 1 raw suppliers

Chemical Property of 1-Adamantyl(4-nitrobenzyl)amine

Chemical Property:

Vapor Pressure:1.13E-07mmHg at 25°C
Boiling Point:432.2°C at 760 mmHg
Flash Point:215.2°C
PSA：57.85000
Density:1.21g/cm³
LogP:4.56730
XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:286.168127949
Heavy Atom Count:21
Complexity:368

Purity/Quality:: 1-ADAMANTYL(4-NITROBENZYL)AMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2CC3CC1CC(C2)(C3)NCC4=CC=C(C=C4)[N+](=O)[O-]

Technology Process of 1-Adamantyl(4-nitrobenzyl)amine

There total 6 articles about 1-Adamantyl(4-nitrobenzyl)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: 89.0%

: 768-94-5
1-Adamantanamine

: 555-16-8
4-nitrobenzaldehdye

: 206053-11-4
(3s,5s,7s)-N-(4-nitrobenzyl)adamantan-1-amine

Guidance literature:: With sodium cyanoborohydride; In methanol; at 20 ℃; Inert atmosphere;
DOI:10.1021/jm301538e

Reference yield: 89.0%

: 206053-11-4
(3s,5s,7s)-N-(4-nitrobenzyl)adamantan-1-amine

Guidance literature:: With sodium cyanoborohydride; In methanol; at 20 ℃; Inert atmosphere;

Reference yield: 70.0%

: 768-94-5
1-Adamantanamine

: 100-11-8
1-bromomethyl-4-nitro-benzene

: 206053-11-4
(3s,5s,7s)-N-(4-nitrobenzyl)adamantan-1-amine

Guidance literature:: With potassium carbonate; In acetonitrile; at 80 ℃; for 24h; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.tet.2017.06.056