4-Methoxy-6-phenyl-5h-pyrimido[4,5-b][1,4]thiazine

Base Information

Chemical Name:4-Methoxy-6-phenyl-5h-pyrimido[4,5-b][1,4]thiazine
CAS No.:1981-06-2
Molecular Formula:C13H11N3OS
Molecular Weight:257.3109
Hs Code.:
NSC Number:75230
DSSTox Substance ID:DTXSID20291397
Wikidata:Q82029351

Synonyms:1981-06-2;NSC75230;4-methoxy-6-phenyl-5h-pyrimido[4,5-b][1,4]thiazine;DTXSID20291397;NSC-75230

Suppliers and Price of 4-Methoxy-6-phenyl-5h-pyrimido[4,5-b][1,4]thiazine

Supply Marketing:

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

Manufacturers and distributors:

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Chemicals and raw materials
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Total 1 raw suppliers

Chemical Property of 4-Methoxy-6-phenyl-5h-pyrimido[4,5-b][1,4]thiazine

Chemical Property:

Vapor Pressure:1.23E-07mmHg at 25°C
Boiling Point:431.2°C at 760 mmHg
Flash Point:214.6°C
Density:1.301g/cm³
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:257.06228316
Heavy Atom Count:18
Complexity:317

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=C2C(=NC=N1)SC=C(N2)C3=CC=CC=C3

Technology Process of 4-Methoxy-6-phenyl-5h-pyrimido[4,5-b][1,4]thiazine

There total 2 articles about 4-Methoxy-6-phenyl-5h-pyrimido[4,5-b][1,4]thiazine 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:

: 32002-69-0
ethyl β-chloro-β-benzoylpyruvate

: 40424-48-4
4-methoxy-5-amino-6-mercaptopyrimidine

: 1981-06-2
4-Methoxy-6-phenylpyrimido<4,5-b>-1,4-thiazine

Guidance literature:: With hydrogenchloride; potassium hydroxide; Yield given. Multistep reaction; 1) EtOH, 20 deg C, 2 h, 2) 1 h;
DOI:10.1007/BF00523072