5-(2-(phenylsulfonyl)ethyl)-1H-indole

Base Information Edit

Chemical Name:5-(2-(phenylsulfonyl)ethyl)-1H-indole
CAS No.:1225327-16-1
Molecular Formula:C₁₆H₁₅NO₂S
Molecular Weight:285.367
Hs Code.:
Mol file:1225327-16-1.mol

Synonyms:5-(2-(phenylsulfonyl)ethyl)-1H-indole

Suppliers and Price of 5-(2-(phenylsulfonyl)ethyl)-1H-indole

Supply Marketing:Edit

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

TRC
Des-dimethylpyrrolidineEletriptan
10mg
$ 105.00

aablocks
5-[2-(benzenesulfonyl)ethyl]-1H-indole 95.0%
100mg
$ 337.00

Total 3 raw suppliers

Chemical Property of 5-(2-(phenylsulfonyl)ethyl)-1H-indole Edit

Chemical Property:

Boiling Point:550.8±42.0 °C(Predicted)
Density:1.292±0.06 g/cm3(Predicted)

Purity/Quality:

90%+ ^*data from raw suppliers

Des-dimethylpyrrolidineEletriptan ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses Des-dimethylpyrrolidine Eletriptan is an impurity of the drug Eletriptan (E505000). Eletriptan is a serotonin 5-HTIB/ID receptor agonist and an antimigraine.

Technology Process of 5-(2-(phenylsulfonyl)ethyl)-1H-indole

There total 11 articles about 5-(2-(phenylsulfonyl)ethyl)-1H-indole 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: 96.0%

: (E)-5-(2-(phenylsulfonyl)vinyl)-1H-indole

: 1225327-16-1
5-(2-(phenylsulfonyl)ethyl)-1H-indole

Guidance literature:: With hydrogen; In toluene; at 80 ℃; for 6.5h; under 1500.15 Torr; Reagent/catalyst; Temperature; Pressure; Catalytic behavior; Schlenk technique; Autoclave; Inert atmosphere;
DOI:10.1007/s10562-020-03407-5