(R)-Thioridazine

Base Information Edit

Chemical Name:(R)-Thioridazine
CAS No.:52496-67-0
Molecular Formula:C₂₁H₂₆N₂S₂
Molecular Weight:370.583
Hs Code.:
Mol file:52496-67-0.mol

Synonyms:(R)-(+)-Thioridazine;(R)-Thioridazine;10H-Phenothiazine, 10-[2-(1-methyl-2-piperidinyl)ethyl]-2-(methylthio)-, (R)-;10H-Phenothiazine, 10-[2-[(2R)-1-methyl-2-piperidinyl]ethyl]-2-(methylthio)- (9CI)

Suppliers and Price of (R)-Thioridazine

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

Total 5 raw suppliers

Chemical Property of (R)-Thioridazine Edit

Chemical Property:

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

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Hazard Codes:

MSDS Files:

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Technology Process of (R)-Thioridazine

There total 25 articles about (R)-Thioridazine 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: 26.0%

: (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-{2-[2-(methylthio)-10H-phenothiazin-10-yl]ethyl}piperidine-1-carboxylate

: 50-52-2,52496-67-0,57129-06-3,114488-10-7
thioridazine

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 0 - 50 ℃; for 18h; Inert atmosphere;

Reference yield:

: 129846-85-1
N-(2-(1-methyl-2-piperidynyl)ethyl)-2-(2-fluorophenylthio)-5-(methylthio)aniline

: 50-52-2,52496-67-0,57129-06-3,114488-10-7
thioridazine

Guidance literature:: With sodium hydride; In dimethyl sulfoxide; for 6.5h; Heating;

Reference yield:

: 1199-36-6
1-chloro-4-(methylthio)-2-nitrobenzene

: 50-52-2,52496-67-0,57129-06-3,114488-10-7
thioridazine

Guidance literature:: Multi-step reaction with 4 steps

1: 89 percent / K₂CO₃ / dimethylformamide / 3.5 h / 60 °C

2: 99 percent / active carbon, N₂H₄, FeCl₃*6H₂O / ethanol / 10 h / Heating

3: 23 percent / 80percent NaH / xylene / 3 h / Heating

4: 80percent NaH / dimethylsulfoxide / 6.5 h / Heating

With iron(III) chloride; sodium hydride; potassium carbonate; pyrographite; hydrazine hydrate; In ethanol; dimethyl sulfoxide; N,N-dimethyl-formamide; xylene;