1H-Pyrido[2,3-b][1,4]thiazin-2(3H)-one

Base Information

Chemical Name:1H-Pyrido[2,3-b][1,4]thiazin-2(3H)-one
CAS No.:18504-81-9
Molecular Formula:C7H6 N2 O S
Molecular Weight:166.203
Hs Code.:2934999090
European Community (EC) Number:242-388-6
UNII:2PL1478Z1W
DSSTox Substance ID:DTXSID60171705
Nikkaji Number:J222.226D
Wikidata:Q27255421
Mol file:18504-81-9.mol

Synonyms:2,3-dihydro-1H-pyridino(2,3-b)(1,4)thiazine-2-one;Abbott 29590

Suppliers and Price of 1H-Pyrido[2,3-b][1,4]thiazin-2(3H)-one

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

TRC
1H,2H,3H-pyrido[2,3-b][1,4]thiazin-2-one
50mg
$ 90.00

Crysdot
1H-Pyrido[2,3-b][1,4]thiazin-2(3H)-one 97%
5g
$ 693.00

Crysdot
1H-Pyrido[2,3-b][1,4]thiazin-2(3H)-one 97%
10g
$ 892.00

Chemcia Scientific
1H-Pyrido[2,3-b][1,4]thiazin-2-one 95%
5 G
$ 785.00

American Custom Chemicals Corporation
1H-PYRIDO[2,3-B][1,4]THIAZIN-2(3H)-ONE 95.00%
5MG
$ 499.69

Total 5 raw suppliers

Chemical Property of 1H-Pyrido[2,3-b][1,4]thiazin-2(3H)-one

Chemical Property:

Vapor Pressure:1.39E-06mmHg at 25°C
Boiling Point:399.2°Cat760mmHg
Flash Point:195.3°C
PSA：70.78000
Density:1.367g/cm³
LogP:1.21090
XLogP3:0.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:166.02008399
Heavy Atom Count:11
Complexity:174

Purity/Quality:

99% ^*data from raw suppliers

1H,2H,3H-pyrido[2,3-b][1,4]thiazin-2-one ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(=O)NC2=C(S1)N=CC=C2

Technology Process of 1H-Pyrido[2,3-b][1,4]thiazin-2(3H)-one

There total 6 articles about 1H-Pyrido[2,3-b][1,4]thiazin-2(3H)-one 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: 69.0%

: 6298-19-7
2-chloro-3-aminopyridine

: 758-08-7
Thioglycolamide

: 18504-81-9
1H-pyrido[2,3-b][1,4]thiazin-2(3H)-one

Guidance literature:: at 100 ℃; for 2h;

Reference yield: 60.0%

: 18504-80-8
2-[(3-nitropyridin-2-yl)sulfanyl]acetic acid

: 18504-81-9
1H-pyrido[2,3-b][1,4]thiazin-2(3H)-one

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; for 5h; under 2585.7 Torr;
DOI:10.1002/(SICI)1521-4184(19991)332:1<19::AID-ARDP19>3.0.CO;2-M