N-benzyl-3-methylphenothiazine

Base Information

Chemical Name:N-benzyl-3-methylphenothiazine
CAS No.:132257-08-0
Molecular Formula:C₂₀H₁₇NS
Molecular Weight:303.428
Hs Code.:

Synonyms:N-benzyl-3-methylphenothiazine

Suppliers and Price of N-benzyl-3-methylphenothiazine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-benzyl-3-methylphenothiazine

Chemical Property:

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Technology Process of N-benzyl-3-methylphenothiazine

There total 8 articles about N-benzyl-3-methylphenothiazine 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: 100.0%

: 132257-05-7
N-benzyl-3-(2,2-diethoxyethylaminomethyl)phenothiazine

: 132257-08-0
N-benzyl-3-methylphenothiazine

Guidance literature:: With cyclohexene; palladium on activated charcoal; In ethanol; for 4.5h; Heating;

Reference yield:

: 92-84-2
10H-phenothiazine

: 132257-08-0
N-benzyl-3-methylphenothiazine

Guidance literature:: Multi-step reaction with 5 steps

1: 42 percent / KOH / dimethylsulfoxide / 2 h / Ambient temperature

2: 14 percent / phosphorus oxychloride / trichloroethene / 2 h / Heating

3: 79 percent / toluene / Heating

4: 14 percent / H₂ / PtO₂ / ethanol / 2 h / Ambient temperature

5: 100 percent / cyclohexene / Pd/C / ethanol / 4.5 h / Heating

With potassium hydroxide; hydrogen; cyclohexene; trichlorophosphate; platinum(IV) oxide; palladium on activated charcoal; In ethanol; Trichloroethylene; dimethyl sulfoxide; toluene;

Reference yield:

: 58478-75-4
10-benzylphenothiazine

: 132257-08-0
N-benzyl-3-methylphenothiazine

Guidance literature:: Multi-step reaction with 4 steps

1: 14 percent / phosphorus oxychloride / trichloroethene / 2 h / Heating

2: 79 percent / toluene / Heating

3: 14 percent / H₂ / PtO₂ / ethanol / 2 h / Ambient temperature

4: 100 percent / cyclohexene / Pd/C / ethanol / 4.5 h / Heating

With hydrogen; cyclohexene; trichlorophosphate; platinum(IV) oxide; palladium on activated charcoal; In ethanol; Trichloroethylene; toluene;