2-endo-hydroxy-4-endo-(methylbenzylamino)noradamantane hydroiodide

Base Information

Chemical Name:2-endo-hydroxy-4-endo-(methylbenzylamino)noradamantane hydroiodide
CAS No.:83916-59-0
Molecular Formula:C₁₇H₂₃NO*HI
Molecular Weight:385.288
Hs Code.:

Synonyms:

Suppliers and Price of 2-endo-hydroxy-4-endo-(methylbenzylamino)noradamantane hydroiodide

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 0 raw suppliers

Chemical Property of 2-endo-hydroxy-4-endo-(methylbenzylamino)noradamantane hydroiodide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-endo-hydroxy-4-endo-(methylbenzylamino)noradamantane hydroiodide

There total 4 articles about 2-endo-hydroxy-4-endo-(methylbenzylamino)noradamantane hydroiodide 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: 72.9%

: 83862-83-3
2-endo-hydroxy-4-endo-(benzylamino)noradamantane

: 74-88-4
methyl iodide

: 83916-59-0
2-endo-hydroxy-4-endo-(methylbenzylamino)noradamantane hydroiodide

Guidance literature:: In diethyl ether; for 240h; Ambient temperature;
DOI:10.1021/jo00148a005

Reference yield:

: 61597-63-5
endo-bicyclo<3.2.1>oct-6-ene-3-carboxaldehyde

: 83916-59-0
2-endo-hydroxy-4-endo-(methylbenzylamino)noradamantane hydroiodide

Guidance literature:: Multi-step reaction with 3 steps

1: 87.1 percent / molecular sieve (4A) / benzene / 48 h / 20 - 25 °C

2: 89.3 percent / Zn, 58percent AcOH / 4 h / 50 - 60 °C

3: 72.9 percent / diethyl ether / 240 h / Ambient temperature

With 4 A molecular sieve; acetic acid; zinc; In diethyl ether; benzene;
DOI:10.1021/jo00148a005

Reference yield:

: 83862-82-2
5-benzyl-4-oxa-5-azatetracyclo<5.3.1.0^2,6.0^3,9>undecane

: 83916-59-0
2-endo-hydroxy-4-endo-(methylbenzylamino)noradamantane hydroiodide

Guidance literature:: Multi-step reaction with 2 steps

1: 89.3 percent / Zn, 58percent AcOH / 4 h / 50 - 60 °C

2: 72.9 percent / diethyl ether / 240 h / Ambient temperature

With acetic acid; zinc; In diethyl ether;
DOI:10.1021/jo00148a005