4-Methyl-2'-methoxybenzothioanilide

Base Information

Chemical Name:4-Methyl-2'-methoxybenzothioanilide
CAS No.:122589-85-9
Molecular Formula:C₁₅H₁₅NOS
Molecular Weight:257.356
Hs Code.:
DSSTox Substance ID:DTXSID301231831

Synonyms:SCHEMBL9620979;WXIVXAWFUYVKHE-UHFFFAOYSA-N;DTXSID301231831;4-methyl-2'-methoxybenzothioanilide;N-(2-methoxyphenyl)-4-methylbenzenecarbothioamide;122589-85-9

Suppliers and Price of 4-Methyl-2'-methoxybenzothioanilide

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 4-Methyl-2'-methoxybenzothioanilide

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:257.08743528
Heavy Atom Count:18
Complexity:274

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(=S)NC2=CC=CC=C2OC

Technology Process of 4-Methyl-2'-methoxybenzothioanilide

There total 4 articles about 4-Methyl-2'-methoxybenzothioanilide 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: 60.0%

: 122589-84-8
N-(2-methoxyphenyl)-4-methyl-benzamide

: 122589-85-9
2'-methoxy-4-methylbenzothioanilide

Guidance literature:: With Lawessons reagent; In toluene; for 1h; Heating;
DOI:10.1248/cpb.40.2387

Reference yield:

: 19172-47-5,94367-93-8
Lawessons reagent

: 122589-85-9
2'-methoxy-4-methylbenzothioanilide

Guidance literature:: In water; toluene;

Reference yield:

: 874-60-2
4-methyl-benzoyl chloride

: 122589-85-9
2'-methoxy-4-methylbenzothioanilide

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / tetrahydrofuran / 1 h / Ambient temperature

2: 60 percent / Lawesson's reagent / toluene / 1 h / Heating

With Lawessons reagent; pyridine; In tetrahydrofuran; toluene;
DOI:10.1248/cpb.40.2387