2-Bromo-10H-phenothiazine

Base Information

Chemical Name:2-Bromo-10H-phenothiazine
CAS No.:66820-95-9
Molecular Formula:C12H8BrNS
Molecular Weight:278.172
Hs Code.:
European Community (EC) Number:927-779-8,827-175-3
DSSTox Substance ID:DTXSID801312367
Nikkaji Number:J586.241H

Synonyms:2-Bromo-10H-phenothiazine;66820-95-9;10H-Phenothiazine, 2-bromo-;2-bromophenothiazine;SCHEMBL9670236;SXBVYXOFICMKHD-UHFFFAOYSA-N;DTXSID801312367;MFCD27921901;AKOS030632164;DS-20115;CS-0100716

Suppliers and Price of 2-Bromo-10H-phenothiazine

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 11 raw suppliers

Chemical Property of 2-Bromo-10H-phenothiazine

Chemical Property:

Vapor Pressure:7E-07mmHg at 25°C
XLogP3:4.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:276.95608
Heavy Atom Count:15
Complexity:236

Purity/Quality:: 99.9% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC3=C(S2)C=CC(=C3)Br

Technology Process of 2-Bromo-10H-phenothiazine

There total 7 articles about 2-Bromo-10H-phenothiazine 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%

: 31928-47-9
4-bromo-2-chloroiodobenzene

: 1204-55-3
thioacetic acid S-(2-acetylamino-phenyl)ester

: 66820-95-9
2-bromo-10H-phenothiazine

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 130 ℃; for 10h; Inert atmosphere;
DOI:10.1080/00397911.2017.1281959

Reference yield: 15.0%

: 20358-03-6
5‐bromo‐1,3‐benzothiazol‐2‐amine

: 583-53-9
2,3-dibromobenzene

: 66820-95-9
2-bromo-10H-phenothiazine

Guidance literature:: With copper(l) iodide; 1,10-Phenanthroline; caesium carbonate; In dimethyl sulfoxide; at 170 ℃; for 24h; Inert atmosphere;
DOI:10.1007/s10593-012-1154-4

Reference yield:

: C₁₂H₉BrClNS*Fe⁽³⁺⁾*C₆H₅O₇^(3-)

: 66820-95-9
2-bromo-10H-phenothiazine

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 110 ℃; regioselective reaction; Green chemistry;
DOI:10.2174/1570178615666180806114523