ethyl 3-phenyl-4H-1,4-benzothiazine-2-carboxylate

Base Information

Chemical Name:ethyl 3-phenyl-4H-1,4-benzothiazine-2-carboxylate
CAS No.:28863-86-7
Molecular Formula:C17H15NO2S
Molecular Weight:297.378
Hs Code.:
DSSTox Substance ID:DTXSID20358833
Wikidata:Q82139704
Mol file:28863-86-7.mol

Synonyms:28863-86-7;4H-1,4-Benzothiazine-2-carboxylic acid, 3-phenyl-, ethyl ester;ethyl 3-phenyl-4H-1,4-benzothiazine-2-carboxylate;DTXSID20358833;4h-1,4-benzothiazine-2-carboxylic acid,3-phenyl-,ethyl ester;AKOS002664176

Suppliers and Price of ethyl 3-phenyl-4H-1,4-benzothiazine-2-carboxylate

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

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Chemical Property of ethyl 3-phenyl-4H-1,4-benzothiazine-2-carboxylate

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:297.08234989
Heavy Atom Count:21
Complexity:415

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1=C(NC2=CC=CC=C2S1)C3=CC=CC=C3

Technology Process of ethyl 3-phenyl-4H-1,4-benzothiazine-2-carboxylate

There total 5 articles about ethyl 3-phenyl-4H-1,4-benzothiazine-2-carboxylate 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: 82.0%

: 94-02-0
ethyl 3-oxo-3-phenylpropionate

: 137-07-5
2-amino-benzenethiol

: 28863-86-7
2-carbethoxy-3-phenyl-4H-<1,4>-benzothiazine

Guidance literature:: With dimethyl sulfoxide; trifluoroacetic acid; at 80 ℃; for 16h;
DOI:10.1002/adsc.202000964

Reference yield: 12.0%

: 2216-94-6
phenylpropynoic acid ethyl ester

: 1141-88-4
2-Aminophenyl disulfide

: 28863-86-7
2-carbethoxy-3-phenyl-4H-<1,4>-benzothiazine

: 883-93-2
2-Phenylbenzothiazole

: 34875-16-6
(E)-Ethyl 1-(2-Aminophenylthio)-1-phenylethylene-2-carboxylate

: 86333-22-4
2-phenyl-2-ethoxycarbonylmethyl-2,3-dihydrobenzothiazole

Guidance literature:: In N,N-dimethyl-formamide; for 15h; Heating;

Reference yield:

: 137-07-5
2-amino-benzenethiol

: 28863-86-7
2-carbethoxy-3-phenyl-4H-<1,4>-benzothiazine

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / air / ethanol

2: 86 percent / dimethylformamide / 15 h / Heating

With air; In ethanol; N,N-dimethyl-formamide;