1-Phenoxyadamantane

Base Information

Chemical Name:1-Phenoxyadamantane
CAS No.:38614-05-0
Molecular Formula:C16H20O
Molecular Weight:228.334
Hs Code.:
NSC Number:111651
DSSTox Substance ID:DTXSID40296809
Nikkaji Number:J1.419.820B
Wikidata:Q82037589
Mol file:38614-05-0.mol

Synonyms:1-phenoxyadamantane;38614-05-0;NSC111651;1-Phenoxy-adamantane;adamantyl phenyl ether;DTXSID40296809;NSC-111651

Suppliers and Price of 1-Phenoxyadamantane

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

Total 16 raw suppliers

Chemical Property of 1-Phenoxyadamantane

Chemical Property:

Vapor Pressure:0.00041mmHg at 25°C
Boiling Point:326.5°C at 760 mmHg
Flash Point:128.6°C
Density:1.12g/cm³
XLogP3:4.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:228.151415257
Heavy Atom Count:17
Complexity:249

Purity/Quality:: 99% ,98%,Electron Grade , ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C2CC3CC1CC(C2)(C3)OC4=CC=CC=C4

Technology Process of 1-Phenoxyadamantane

There total 8 articles about 1-Phenoxyadamantane 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%

: tetraphenylbismuth(V) fluoride

: 768-95-6
1-adamanthanol

: 38614-05-0
(3s,5s,7s)-1-phenoxyadamantane

Guidance literature:: With N-Methyldicyclohexylamine; copper diacetate; In toluene; at 20 ℃; for 1h;
DOI:10.1246/cl.2006.1140

Reference yield: 59.0%

: 768-95-6
1-adamanthanol

: 66003-78-9,130595-32-3,220122-79-2
triphenylsulfonium trifluoromethanesulfonate

: 38614-05-0
(3s,5s,7s)-1-phenoxyadamantane

Guidance literature:: With sodium hydride; In 1,4-dioxane; at 50 ℃; for 24h; Reagent/catalyst; Inert atmosphere; Glovebox;
DOI:10.1002/asia.201900968

Reference yield:

: 768-95-6
1-adamanthanol

: 38614-05-0
(3s,5s,7s)-1-phenoxyadamantane

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / dichloromethane / 1 h / 0 - 20 °C / Schlenk technique; Inert atmosphere

2: di-isopropyl azodicarboxylate / dichloromethane / 0.25 h / 20 °C / Inert atmosphere; Schlenk technique

With pyridine; di-isopropyl azodicarboxylate; In dichloromethane;
DOI:10.1021/acs.orglett.2c00042