6,7-Dimethoxy-4-(4-methylphenyl)-2H-1,3-benzothiazine

Base Information

Chemical Name:6,7-Dimethoxy-4-(4-methylphenyl)-2H-1,3-benzothiazine
CAS No.:91937-65-4
Molecular Formula:C17H17NO2S
Molecular Weight:299.393
Hs Code.:
DSSTox Substance ID:DTXSID30533518
Nikkaji Number:J2.845.767G
Wikidata:Q82406886

Synonyms:91937-65-4;6,7-Dimethoxy-4-(4-methylphenyl)-2H-1,3-benzothiazine;DTXSID30533518

Suppliers and Price of 6,7-Dimethoxy-4-(4-methylphenyl)-2H-1,3-benzothiazine

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 6,7-Dimethoxy-4-(4-methylphenyl)-2H-1,3-benzothiazine

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:299.09799996
Heavy Atom Count:21
Complexity:379

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C2=NCSC3=CC(=C(C=C32)OC)OC

Technology Process of 6,7-Dimethoxy-4-(4-methylphenyl)-2H-1,3-benzothiazine

There total 3 articles about 6,7-Dimethoxy-4-(4-methylphenyl)-2H-1,3-benzothiazine 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:

: 1233241-26-3
C₁₉H₁₇Cl₂NO₃S

: 91937-65-4
6,7-Dimethoxy-4-p-tolyl-2H-benzo[e][1,3]thiazine

Guidance literature:: With sodium methylate; In methanol; for 0.25h; Reflux;
DOI:10.1016/j.tetlet.2010.04.051

Reference yield:

: 700-96-9
3,4-dimethoxythiophenol

: 91937-65-4
6,7-Dimethoxy-4-p-tolyl-2H-benzo[e][1,3]thiazine

Guidance literature:: Multi-step reaction with 2 steps

1: 84.5 percent / HCl / ethanol

2: 3.3 percent / POCl₃ / 1 h / Heating

With hydrogenchloride; trichlorophosphate; In ethanol;

Reference yield:

: 31220-71-0
N-(hydroxymethyl)-4-methylbenzamide

: 91937-65-4
6,7-Dimethoxy-4-p-tolyl-2H-benzo[e][1,3]thiazine

Guidance literature:: Multi-step reaction with 2 steps

1: 84.5 percent / HCl / ethanol

2: 3.3 percent / POCl₃ / 1 h / Heating

With hydrogenchloride; trichlorophosphate; In ethanol;