4-phenyl-4H-3,1-benzothiazin-2-amine

Base Information

Chemical Name:4-phenyl-4H-3,1-benzothiazin-2-amine
CAS No.:16781-33-2
Molecular Formula:C₁₄H₁₂N₂S
Molecular Weight:240.329
Hs Code.:
DSSTox Substance ID:DTXSID001291876

Synonyms:4-phenyl-4H-3,1-benzothiazin-2-amine;SCHEMBL24287277;DTXSID001291876;16781-33-2;(4-phenyl-4H-[3,1]benzothiazin-2-yl)-amine

Suppliers and Price of 4-phenyl-4H-3,1-benzothiazin-2-amine

Supply Marketing:

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

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Chemical Property of 4-phenyl-4H-3,1-benzothiazin-2-amine

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:240.07211956
Heavy Atom Count:17
Complexity:297

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2C3=CC=CC=C3N=C(S2)N

Technology Process of 4-phenyl-4H-3,1-benzothiazin-2-amine

There total 2 articles about 4-phenyl-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: 80.0%

: 13209-38-6
(2-aminophenyl)(phenyl)methanol

: 17356-08-0
thiourea

: 16781-33-2
2-Amino-4-phenyl-4H-3,1-benzothiazine

Guidance literature:: With hydrogen bromide; for 1.5h; Heating;
DOI:10.1002/jhet.5570210432

Reference yield:

: 16781-33-2
2-Amino-4-phenyl-4H-3,1-benzothiazine

Guidance literature:: 2-Aminobenzhydrol, Thioharnstoff;

Reference yield:

: 16781-33-2
2-Amino-4-phenyl-4H-3,1-benzothiazine

: 93765-01-6
5-Phenyl-5H-4-thia-3,9b-diaza-cyclopenta[a]naphthalene-2-carboxylic acid ethyl ester; hydrobromide

Guidance literature:: Multi-step reaction with 2 steps

1: 37 percent / 1,2-dimethoxy-ethane / 24 h / Ambient temperature

2: 96 percent / ethanol / 1.5 h / Heating

In 1,2-dimethoxyethane; ethanol;
DOI:10.1002/jhet.5570210432