3-Methyl-2-(3-methyl-2-benzothiazolinylidene)methylbenzothiazolium iodide

Base Information

Chemical Name:3-Methyl-2-(3-methyl-2-benzothiazolinylidene)methylbenzothiazolium iodide
CAS No.:2783-72-4
Molecular Formula:C17H15 N2 S2 . I
Molecular Weight:438.356
Hs Code.:

Synonyms:3,3'-Dimethylmonomethinethiacyanine iodide;3-Methyl-2-(3-methyl-2-benzothiazolinylidene)methylbenzothiazolium iodide;BENZOTHIAZOLIUM, 3-METHYL-2-(3-METHYL-2-BENZOTHIAZOLINYLIDENE)METHYL-, IODIDE;C17H15N2S2.I;2783-72-4;C17-H15-N2-S2.I;LS-40900;Benzothiazolium, 3-methyl-2-[(3-methyl-2(3H)-benzothiazolylidene)methyl]-, iodide

Suppliers and Price of 3-Methyl-2-(3-methyl-2-benzothiazolinylidene)methylbenzothiazolium iodide

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 3-Methyl-2-(3-methyl-2-benzothiazolinylidene)methylbenzothiazolium iodide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:437.97214
Heavy Atom Count:22
Complexity:387

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2=CC=CC=C2SC1=CC3=[N+](C4=CC=CC=C4S3)C.[I-]
Isomeric SMILES:CN\1C2=CC=CC=C2S/C1=C\C3=[N+](C4=CC=CC=C4S3)C.[I-]

Technology Process of 3-Methyl-2-(3-methyl-2-benzothiazolinylidene)methylbenzothiazolium iodide

There total 13 articles about 3-Methyl-2-(3-methyl-2-benzothiazolinylidene)methylbenzothiazolium iodide 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: 81.0%

: 27825-90-7
3-methyl-2-methylthiobenzothiazolium methylsulfate

: 2038-15-5
2,3-dimethylbenzothiazolium methosulfate

: 2783-72-4
bis-(3-methyl-benzothiazol-2-yl)-methinium; iodide

Guidance literature:: 3-methyl-2-methylthiobenzothiazolium methylsulfate; 2,3-dimethylbenzothiazolium methosulfate; With acetic anhydride; N-ethyl-N,N-diisopropylamine; for 0.25h; Reflux;

With potassium iodide; In water;
DOI:10.1039/d1nj01659h

Reference yield:

: 16021-56-0
1,2,2-trimethyl-1,2-dihydroquinoline

: 4329-95-7
3-Methylbenzothiazolium 2-sulfonate

: 16768-72-2
1-methyl-2-(3-methyl-3H-benzothiazol-2-ylidenemethyl)-quinolinium; iodide

: 2783-72-4
bis-(3-methyl-benzothiazol-2-yl)-methinium; iodide

Guidance literature:: With sodium iodide; In ethanol; for 4h; Heating;

Reference yield:

: 120-75-2
2-Methylbenzothiazole

: 2783-72-4
bis-(3-methyl-benzothiazol-2-yl)-methinium; iodide

Guidance literature:: Multi-step reaction with 2 steps

1: neat (no solvent) / 1 h / 90 °C / Inert atmosphere

2: acetic anhydride; N-ethyl-N,N-diisopropylamine / 0.25 h / Reflux

With acetic anhydride; N-ethyl-N,N-diisopropylamine; In neat (no solvent);
DOI:10.1039/d1nj01659h