(2H-1,4-benzothiazin-3(4H)-ylidene)<3-(trifluoromethyl)phenyl>acetonitrile

Base Information

Chemical Name:(2H-1,4-benzothiazin-3(4H)-ylidene)<3-(trifluoromethyl)phenyl>acetonitrile
CAS No.:84590-70-5
Molecular Formula:C₁₇H₁₁F₃N₂S
Molecular Weight:332.349
Hs Code.:

Synonyms:(2H-1,4-benzothiazin-3(4H)-ylidene)<3-(trifluoromethyl)phenyl>acetonitrile

Suppliers and Price of (2H-1,4-benzothiazin-3(4H)-ylidene)<3-(trifluoromethyl)phenyl>acetonitrile

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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 (2H-1,4-benzothiazin-3(4H)-ylidene)<3-(trifluoromethyl)phenyl>acetonitrile

Chemical Property:

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Technology Process of (2H-1,4-benzothiazin-3(4H)-ylidene)<3-(trifluoromethyl)phenyl>acetonitrile

There total 1 articles about (2H-1,4-benzothiazin-3(4H)-ylidene)<3-(trifluoromethyl)phenyl>acetonitrile 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:

: 2338-76-3
3-trifluoromethylphenylacetonitrile

: 140-53-4
p-chlorobenzyl cyanide

: 84590-70-5
(2H-1,4-benzothiazin-3(4H)-ylidene)<3-(trifluoromethyl)phenyl>acetonitrile

Guidance literature:

Reference yield: 88.0%

: 84590-70-5
(2H-1,4-benzothiazin-3(4H)-ylidene)<3-(trifluoromethyl)phenyl>acetonitrile

: 84590-75-0
2-(2H-1,4-benzothiazin-3(4H)-ylidene)-2-<3-(trifluromethyl)phenyl>acetamide

Guidance literature:: With sulfuric acid; water; for 2.5h; Ambient temperature;
DOI:10.1021/jo00383a044

Reference yield:

: 84590-70-5
(2H-1,4-benzothiazin-3(4H)-ylidene)<3-(trifluoromethyl)phenyl>acetonitrile

: 2-[4H-Benzo[1,4]thiazin-(3Z)-ylidene]-N-[1-dimethylamino-meth-(E)-ylidene]-2-(3-trifluoromethyl-phenyl)-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / conc. H₂SO₄, H₂O / 2.5 h / Ambient temperature

2: dimethylformamide / 2 h / Ambient temperature

With sulfuric acid; water; In N,N-dimethyl-formamide;
DOI:10.1021/jo00383a044