4-<(triphenylmethyl)amino>-1-<4-amino>butyl>-2(1H)-pyrimidinone

Base Information

Chemical Name:4-<(triphenylmethyl)amino>-1-<4-amino>butyl>-2(1H)-pyrimidinone
CAS No.:130798-37-7
Molecular Formula:C₃₉H₅₄N₆O
Molecular Weight:622.897
Hs Code.:

4-<(triphenylmethyl)amino>-1-<4-<N,N-bis<2-(N,N-diethylamino)ethyl>amino>butyl>-2(1H)-pyrimidinone

Synonyms:4-<(triphenylmethyl)amino>-1-<4-amino>butyl>-2(1H)-pyrimidinone

Suppliers and Price of 4-<(triphenylmethyl)amino>-1-<4-amino>butyl>-2(1H)-pyrimidinone

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 4-<(triphenylmethyl)amino>-1-<4-amino>butyl>-2(1H)-pyrimidinone

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-<(triphenylmethyl)amino>-1-<4-amino>butyl>-2(1H)-pyrimidinone

There total 5 articles about 4-<(triphenylmethyl)amino>-1-<4-amino>butyl>-2(1H)-pyrimidinone 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%

: 123-12-6
N,N,N',N'-tetraethyldiethylenetriamine

: 130798-27-5
1-(4-iodobutyl)-N⁴-tritylcytosine

: 130798-37-7
4-<(triphenylmethyl)amino>-1-<4-amino>butyl>-2(1H)-pyrimidinone

Guidance literature:: With potassium carbonate; In acetonitrile; for 24h; Ambient temperature;
DOI:10.1021/ja00003a035

Reference yield:

: 596-43-0
bromo-triphenyl-methane

: 130798-37-7
4-<(triphenylmethyl)amino>-1-<4-amino>butyl>-2(1H)-pyrimidinone

Guidance literature:: Multi-step reaction with 3 steps

1: 68 percent / pyridine / 24 h / 90 °C

3: 93 percent / K₂CO₃ / acetonitrile / 24 h / Ambient temperature

With pyridine; potassium carbonate; In acetonitrile;
DOI:10.1021/ja00003a035

Reference yield:

: 130798-21-9
1-butenylcytosine

: 130798-37-7
4-<(triphenylmethyl)amino>-1-<4-amino>butyl>-2(1H)-pyrimidinone

Guidance literature:: Multi-step reaction with 3 steps

1: 68 percent / pyridine / 24 h / 90 °C

3: 93 percent / K₂CO₃ / acetonitrile / 24 h / Ambient temperature

With pyridine; potassium carbonate; In acetonitrile;
DOI:10.1021/ja00003a035