10H-Phenothiazine-3-carboxylic acid

Base Information

Chemical Name:10H-Phenothiazine-3-carboxylic acid
CAS No.:68230-59-1
Molecular Formula:C13H9NO2S
Molecular Weight:243.2811
Hs Code.:
NSC Number:158946
DSSTox Substance ID:DTXSID10987752
Nikkaji Number:J3.069.968H
Wikidata:Q82976076

Synonyms:10H-Phenothiazine-3-carboxylic acid;68230-59-1;Phenothiazine-3-carboxylic acid;SCHEMBL5121603;DTXSID10987752;NSC158946;AKOS037645673;NSC-158946;10H-Phenothiazine-3-carboxylic acid #;AS-62103;D93243

Suppliers and Price of 10H-Phenothiazine-3-carboxylic acid

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 6 raw suppliers

Chemical Property of 10H-Phenothiazine-3-carboxylic acid

Chemical Property:

Vapor Pressure:3.47E-10mmHg at 25°C
Boiling Point:484.2°Cat760mmHg
Flash Point:246.6°C
Density:1.397g/cm³
XLogP3:3.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:243.03539970
Heavy Atom Count:17
Complexity:310

Purity/Quality:: 99% ^*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=C(C=C3)C(=O)O

Technology Process of 10H-Phenothiazine-3-carboxylic acid

There total 5 articles about 10H-Phenothiazine-3-carboxylic acid 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: 78.0%

: 42860-10-6
3-bromo-4-chlorobenzoic acid

: 137-07-5
2-amino-benzenethiol

: 68230-59-1
10H-phenothiazine-3-carboxylic acid

Guidance literature:: With copper(l) iodide; potassium carbonate; In dimethyl sulfoxide; at 120 ℃; for 48h; regioselective reaction; Inert atmosphere;
DOI:10.1039/c2cc30814b

Reference yield: 43.0%

: 494799-27-8
ethyl 4-acetamido-3-iodobenzoate

: 6320-02-1
o-bromothiophenol

: C₁₅H₁₃NO₂S

: 68230-59-1
10H-phenothiazine-3-carboxylic acid

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 135 ℃; for 48h; Inert atmosphere; Green chemistry;
DOI:10.1039/c6ra01295g

Reference yield: 42.0%

: 6320-03-2
2-chlorothiphenol

: 494799-27-8
ethyl 4-acetamido-3-iodobenzoate

: C₁₅H₁₃NO₂S

: 68230-59-1
10H-phenothiazine-3-carboxylic acid

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 135 ℃; for 48h; Inert atmosphere; Green chemistry;
DOI:10.1039/c6ra01295g