N-Acetylphenoxazine

Base Information

Chemical Name:N-Acetylphenoxazine
CAS No.:6192-43-4
Molecular Formula:C14H11NO2
Molecular Weight:225.247
Hs Code.:
UNII:VVA9DLS3TV
DSSTox Substance ID:DTXSID10210951
Nikkaji Number:J3.068.499K
Wikidata:Q27292034
ChEMBL ID:CHEMBL2180182

Synonyms:HJ-PI01

Suppliers and Price of N-Acetylphenoxazine

Supply Marketing:

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 7 raw suppliers

Chemical Property of N-Acetylphenoxazine

Chemical Property:

PSA：29.54000
LogP:3.54190
XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:225.078978594
Heavy Atom Count:17
Complexity:283

Purity/Quality:: 98%+ ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)N1C2=CC=CC=C2OC3=CC=CC=C31

Technology Process of N-Acetylphenoxazine

There total 5 articles about N-Acetylphenoxazine 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: 27.0%

: 204847-21-2
N-(2-(2-bromophenoxy)phenyl)acetamide

: 6192-43-4
1-(10H-phenoxazin-10-yl)ethan-1-one

: 135-67-1
phenoxazine

Guidance literature:: With sodium carbonate; In N,N-dimethyl-formamide; at 155 ℃; for 0.25h; Reagent/catalyst; Temperature; Microwave irradiation;
DOI:10.1080/00397911.2020.1849723

Reference yield:

: 1493-27-2,127723-77-7
ortho-nitrofluorobenzene

: 6192-43-4
1-(10H-phenoxazin-10-yl)ethan-1-one

: 135-67-1
phenoxazine

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate / N,N-dimethyl-formamide / 3 h / 0 - 80 °C

2: tin(II) chloride dihdyrate / ethyl acetate / 18 h / 20 °C

3: pyridine / dichloromethane / 4 h / 0 - 20 °C

4: sodium carbonate / N,N-dimethyl-formamide / 0.25 h / 155 °C / Microwave irradiation

With pyridine; tin(II) chloride dihdyrate; sodium carbonate; caesium carbonate; In dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1080/00397911.2020.1849723

Reference yield:

: 70787-31-4
2-amino-2'-bromo-diphenyl ether

: 6192-43-4
1-(10H-phenoxazin-10-yl)ethan-1-one

: 135-67-1
phenoxazine

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / dichloromethane / 4 h / 0 - 20 °C

2: sodium carbonate / N,N-dimethyl-formamide / 0.25 h / 155 °C / Microwave irradiation

With pyridine; sodium carbonate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1080/00397911.2020.1849723