N⁶-(1-phenyl-2(S)-propyl)-9-phenyladenine

Base Information

Chemical Name:N⁶-(1-phenyl-2(S)-propyl)-9-phenyladenine
CAS No.:135426-10-7
Molecular Formula:C₂₀H₁₉N₅
Molecular Weight:329.404
Hs Code.:

N<sup>6</sup>-(1-phenyl-2(S)-propyl)-9-phenyladenine

Synonyms:N⁶-(1-phenyl-2(S)-propyl)-9-phenyladenine

Suppliers and Price of N⁶-(1-phenyl-2(S)-propyl)-9-phenyladenine

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 N⁶-(1-phenyl-2(S)-propyl)-9-phenyladenine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N⁶-(1-phenyl-2(S)-propyl)-9-phenyladenine

There total 2 articles about N⁶-(1-phenyl-2(S)-propyl)-9-phenyladenine 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: 93.0%

: 5470-24-6
6-Chloro-9-phenyl-9H-purine

: 51-64-9,17108-96-2,96332-84-2
dexamfetamine

: 135426-10-7
N⁶-(1-phenyl-2(S)-propyl)-9-phenyladenine

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In propan-1-ol; for 24h; Heating;
DOI:10.1021/jm00113a029

Reference yield:

: 41259-65-8
6-chloro-N₄-phenylpyrimidine-4,5-diamine

: 135426-10-7
N⁶-(1-phenyl-2(S)-propyl)-9-phenyladenine

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / ethanesulfonic acid / 48 h / Ambient temperature

2: 93 percent / N,N-diisopropylethylamine / propan-1-ol / 24 h / Heating

With ethanesulfonic acid; N-ethyl-N,N-diisopropylamine; In propan-1-ol;
DOI:10.1021/jm00113a029