N-(3-Chlorophenyl)-4H-3,1-benzothiazin-2-amine

Base Information

Chemical Name:N-(3-Chlorophenyl)-4H-3,1-benzothiazin-2-amine
CAS No.:62348-11-2
Molecular Formula:C₁₄H₁₁ClN₂S
Molecular Weight:274.774
Hs Code.:
DSSTox Substance ID:DTXSID40547500
Wikidata:Q82425761

Synonyms:N-(3-Chlorophenyl)-4H-3,1-benzothiazin-2-amine;62348-11-2;SCHEMBL11741665;DTXSID40547500

Suppliers and Price of N-(3-Chlorophenyl)-4H-3,1-benzothiazin-2-amine

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 N-(3-Chlorophenyl)-4H-3,1-benzothiazin-2-amine

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:274.0331472
Heavy Atom Count:18
Complexity:321

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C2=CC=CC=C2N=C(S1)NC3=CC(=CC=C3)Cl

Technology Process of N-(3-Chlorophenyl)-4H-3,1-benzothiazin-2-amine

There total 5 articles about N-(3-Chlorophenyl)-4H-3,1-benzothiazin-2-amine 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:

: 62348-10-1
2-methylsulfanyl-4H-benzo[d][1,3]thiazine

: 108-42-9
3-chloro-aniline

: 62348-11-2
2-(3-chloroanilino)-4H-3,1-benzothiazine

Guidance literature:: In butan-1-ol;

Reference yield:

: 109768-52-7
1-{2-[3-(3-Chloro-phenyl)-thioureido]-benzyl}-pyridinium; bromide

: 62348-11-2
2-(3-chloroanilino)-4H-3,1-benzothiazine

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / KOH / methanol / 4 h

2: 88 percent / dimethylformamide / 0.02 h / Heating

With potassium hydroxide; In methanol; N,N-dimethyl-formamide;

Reference yield:

: 108288-40-0
2-(bromomethyl)phenyl isothiocyanate

: 62348-11-2
2-(3-chloroanilino)-4H-3,1-benzothiazine

Guidance literature:: Multi-step reaction with 4 steps

1: 87 percent / diethyl ether / 48 h

2: 100 percent / methanol / 5 h

3: 88 percent / KOH / methanol / 4 h

4: 88 percent / dimethylformamide / 0.02 h / Heating

With potassium hydroxide; In methanol; diethyl ether; N,N-dimethyl-formamide;