N-(5-Hydroxy-12H-benzo[a]phenothiazin-6-yl)-N-phenylacetamide

Base Information

Chemical Name:N-(5-Hydroxy-12H-benzo[a]phenothiazin-6-yl)-N-phenylacetamide
CAS No.:91757-14-1
Molecular Formula:C24H18N2O2S
Molecular Weight:398.485
Hs Code.:
DSSTox Substance ID:DTXSID20525846

Synonyms:91757-14-1;N-(5-Hydroxy-12H-benzo[a]phenothiazin-6-yl)-N-phenylacetamide;DTXSID20525846

Suppliers and Price of N-(5-Hydroxy-12H-benzo[a]phenothiazin-6-yl)-N-phenylacetamide

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of N-(5-Hydroxy-12H-benzo[a]phenothiazin-6-yl)-N-phenylacetamide

Chemical Property:

XLogP3:5.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:398.10889899
Heavy Atom Count:29
Complexity:595

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)N(C1=CC=CC=C1)C2=C(C3=CC=CC=C3C4=C2SC5=CC=CC=C5N4)O

Technology Process of N-(5-Hydroxy-12H-benzo[a]phenothiazin-6-yl)-N-phenylacetamide

There total 5 articles about N-(5-Hydroxy-12H-benzo[a]phenothiazin-6-yl)-N-phenylacetamide 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: 72.0%

: 25947-10-8
6-N-(acetylanilino)-5H-benzo phenothiazin-5-one

: 91757-14-1
6-N-(acetylanilino)-12H-benzo phenothiazin-5-ol

Guidance literature:: With acetic anhydride; zinc; In ethanol; for 0.5h; Heating;

Reference yield:

: 1090-16-0
2-chloro-3-(phenylamino)naphthalene-1,4-dione

: 91757-14-1
6-N-(acetylanilino)-12H-benzo phenothiazin-5-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / conc. H₂SO₄ / 1.5 h / 80 °C

2: 80 percent / ethanol / 2 h / Heating

3: 72 percent / zinc dust, acetanhydride / ethanol / 0.5 h / Heating

With sulfuric acid; acetic anhydride; zinc; In ethanol;

Reference yield:

: 4497-73-8
N-(3-chloro-1,4-dioxo-1,4-dihydronaphthalen-2-yl)-N-phenylacetamide

: 91757-14-1
6-N-(acetylanilino)-12H-benzo phenothiazin-5-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 80 percent / ethanol / 2 h / Heating

2: 72 percent / zinc dust, acetanhydride / ethanol / 0.5 h / Heating

With acetic anhydride; zinc; In ethanol;