(2E)-2-(3-methyl-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)-4H-1,4-benzothiazin-3-one

Base Information

Chemical Name:(2E)-2-(3-methyl-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)-4H-1,4-benzothiazin-3-one
CAS No.:54255-34-4
Molecular Formula:C12H8N2O2S3
Molecular Weight:308.3991
Hs Code.:
NSC Number:303570
DSSTox Substance ID:DTXSID80419474
Wikidata:Q82230481

Synonyms:NSC303570;54255-34-4;DTXSID80419474;NSC-303570

Suppliers and Price of (2E)-2-(3-methyl-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)-4H-1,4-benzothiazin-3-one

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 2 raw suppliers

Chemical Property of (2E)-2-(3-methyl-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)-4H-1,4-benzothiazin-3-one

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.66g/cm³
XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:0
Exact Mass:307.97479102
Heavy Atom Count:19
Complexity:503

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C(=O)C(=C2C(=O)NC3=CC=CC=C3S2)SC1=S
Isomeric SMILES:CN1C(=O)/C(=C\2/C(=O)NC3=CC=CC=C3S2)/SC1=S

Technology Process of (2E)-2-(3-methyl-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)-4H-1,4-benzothiazin-3-one

There total 3 articles about (2E)-2-(3-methyl-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)-4H-1,4-benzothiazin-3-one 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:

: 54326-51-1
2-(3-methyl-4-oxo-2-thioxo-thiazolidin-5-yl)-4H-benzo[1,4]thiazin-3-one

: 54255-34-4
2-((E)-3-methyl-4-oxo-2-thioxo-thiazolidin-5-ylidene)-4H-benzo[1,4]thiazin-3-one

Guidance literature:: With bromine; In acetic acid;
DOI:10.1248/cpb.22.42

Reference yield:

: 41270-29-5
(3-methyl-4-oxo-2-thioxo-thiazolidin-5-ylidene)-acetic acid methyl ester

: 54255-34-4
2-((E)-3-methyl-4-oxo-2-thioxo-thiazolidin-5-ylidene)-4H-benzo[1,4]thiazin-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: methanol

2: Br₂ / acetic acid

With bromine; In methanol; acetic acid;
DOI:10.1248/cpb.22.42

Reference yield:

: 137-07-5
2-amino-benzenethiol

: 54255-34-4
2-((E)-3-methyl-4-oxo-2-thioxo-thiazolidin-5-ylidene)-4H-benzo[1,4]thiazin-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: methanol

2: Br₂ / acetic acid

With bromine; In methanol; acetic acid;
DOI:10.1248/cpb.22.42