10H-Phenothiazine, 10-((2-naphthalenyloxy)acetyl)-

Base Information

Chemical Name:10H-Phenothiazine, 10-((2-naphthalenyloxy)acetyl)-
CAS No.:136801-31-5
Molecular Formula:C24H17NO2S
Molecular Weight:383.4623
Hs Code.:
DSSTox Substance ID:DTXSID90159935
Wikidata:Q83028308
ChEMBL ID:CHEMBL1566175

Synonyms:136801-31-5;10-((2-Naphthalenyloxy)acetyl)-10H-phenothiazine;10H-Phenothiazine, 10-((2-naphthalenyloxy)acetyl)-;BRN 4884641;10-[(2-naphthyloxy)acetyl]-10H-phenothiazine;2-(naphthalen-2-yloxy)-1-(10H-phenothiazin-10-yl)ethanone;CDS1_005001;CBMicro_036745;Oprea1_505846;MLS000571361;DivK1c_006041;CHEMBL1566175;DTXSID90159935;HMS2447B23;STK032125;AKOS001639233;NCGC00245768-01;SMR000193446;BIM-0036676.P001;LS-105624;EU-0075284;SR-01000465623;SR-01000465623-1

Suppliers and Price of 10H-Phenothiazine, 10-((2-naphthalenyloxy)acetyl)-

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 0 raw suppliers

Chemical Property of 10H-Phenothiazine, 10-((2-naphthalenyloxy)acetyl)-

Chemical Property:

Vapor Pressure:4.2E-17mmHg at 25°C
Boiling Point:656.3°Cat760mmHg
Flash Point:350.7°C
Density:1.32g/cm³
XLogP3:5.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:383.09799996
Heavy Atom Count:28
Complexity:533

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C=C(C=CC2=C1)OCC(=O)N3C4=CC=CC=C4SC5=CC=CC=C53

Technology Process of 10H-Phenothiazine, 10-((2-naphthalenyloxy)acetyl)-

There total 2 articles about 10H-Phenothiazine, 10-((2-naphthalenyloxy)acetyl)- 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: 60.0%

: 92-84-2
10H-phenothiazine

: 40926-77-0
(2-naphthyloxy)acetyl chloride

: 136801-31-5
2-(Naphthalen-2-yloxy)-1-phenothiazin-10-yl-ethanone

Guidance literature:: With sodium hydroxide; In methanol; diethyl ether; ethyl acetate;

Reference yield:

: 120-23-0
(2-naphthoyl)oxyacetic acid

: 136801-31-5
2-(Naphthalen-2-yloxy)-1-phenothiazin-10-yl-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / benzene; ethyl acetate; methanol / 8 h / Heating

2: 60 percent / 4N NaOH / ethyl acetate; methanol; diethyl ether

With sodium hydroxide; thionyl chloride; In methanol; diethyl ether; ethyl acetate; benzene;