10H-Phenothiazine-2-carbonitrile, 10-[2-methyl-3-(methylamino)propyl]-

Base Information

Chemical Name:10H-Phenothiazine-2-carbonitrile, 10-[2-methyl-3-(methylamino)propyl]-
CAS No.:108014-19-3
Molecular Formula:C18H19N3S
Molecular Weight:309.435
Hs Code.:
DSSTox Substance ID:DTXSID90439385
Nikkaji Number:J1.531.011A
Mol file:108014-19-3.mol

Synonyms:108014-19-3;10H-Phenothiazine-2-carbonitrile, 10-[2-methyl-3-(methylamino)propyl]-;SCHEMBL2639793;DTXSID90439385;2-Cyano-10-[3-(methylamino)-2-methylpropyl]-10H-phenothiazine

Suppliers and Price of 10H-Phenothiazine-2-carbonitrile, 10-[2-methyl-3-(methylamino)propyl]-

Supply Marketing:

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

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Chemical Property of 10H-Phenothiazine-2-carbonitrile, 10-[2-methyl-3-(methylamino)propyl]-

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:309.12996879
Heavy Atom Count:22
Complexity:418

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(CNC)CN1C2=CC=CC=C2SC3=C1C=C(C=C3)C#N

Technology Process of 10H-Phenothiazine-2-carbonitrile, 10-[2-methyl-3-(methylamino)propyl]-

There total 2 articles about 10H-Phenothiazine-2-carbonitrile, 10-[2-methyl-3-(methylamino)propyl]- 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: 70.0%

: 1366180-94-0
cyamemazine N-oxide

: 108014-19-3
N-Demethylcyamemazine

: 3546-03-0
cyamemazine

Guidance literature:: With ferrous(II) sulfate heptahydrate; In methanol; at 0 ℃; for 2h;
DOI:10.1016/j.bmcl.2012.01.131

Reference yield:

: Cyamemazine tartrate

: 108014-19-3
N-Demethylcyamemazine

: 3546-03-0
cyamemazine

Guidance literature:: Multi-step reaction with 2 steps

1: 3-chloro-benzenecarboperoxoic acid; sodium hydroxide / dichloromethane / 4 h / 0 - 20 °C

2: ferrous(II) sulfate heptahydrate / methanol / 2 h / 0 °C

With ferrous(II) sulfate heptahydrate; 3-chloro-benzenecarboperoxoic acid; sodium hydroxide; In methanol; dichloromethane; 2: Polonovski reaction;
DOI:10.1016/j.bmcl.2012.01.131