Aethandithiophosphonsaeure O-methyl-S-((oxazolo(4,5-b)pyridin-2(3H)-on-3-yl)methyl) ester

Base Information

Chemical Name:Aethandithiophosphonsaeure O-methyl-S-((oxazolo(4,5-b)pyridin-2(3H)-on-3-yl)methyl) ester
CAS No.:54253-87-1
Molecular Formula:C10H13N2O3PS2
Molecular Weight:304.3256
Hs Code.:
DSSTox Substance ID:DTXSID60969260

Synonyms:BRN 1082436;Aethandithiophosphonsaeure O-methyl-S-((oxazolo(4,5-b)pyridin-2(3H)-on-3-yl)methyl) ester;54253-87-1;Phosphonodithioic acid, ethyl-, O-methyl ester, S-ester with 3-(mercaptomethyl)oxazolo(4,5-b)pyridin-2(3H)-one;C10H13N2O3PS2;DTXSID60969260;C10-H13-N2-O3-P-S2;LS-106997;O-Methyl S-[(2-oxo[1,3]oxazolo[4,5-b]pyridin-3(2H)-yl)methyl] ethylphosphonodithioate

Suppliers and Price of Aethandithiophosphonsaeure O-methyl-S-((oxazolo(4,5-b)pyridin-2(3H)-on-3-yl)methyl) ester

Supply Marketing:

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

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Chemical Property of Aethandithiophosphonsaeure O-methyl-S-((oxazolo(4,5-b)pyridin-2(3H)-on-3-yl)methyl) ester

Chemical Property:

Vapor Pressure:1.9E-07mmHg at 25°C
Boiling Point:425.5°Cat760mmHg
Flash Point:211.1°C
Density:1.426g/cm³
XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:304.01052163
Heavy Atom Count:18
Complexity:369

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCP(=S)(OC)SCN1C2=C(C=CC=N2)OC1=O

Technology Process of Aethandithiophosphonsaeure O-methyl-S-((oxazolo(4,5-b)pyridin-2(3H)-on-3-yl)methyl) ester

There total 5 articles about Aethandithiophosphonsaeure O-methyl-S-((oxazolo(4,5-b)pyridin-2(3H)-on-3-yl)methyl) ester 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:

: 35570-62-8
3-hydroxymethyl-3H-oxazolo[4,5-b]pyridin-2-one

: 54253-87-1
ethyl-phosphonodithioic acid O-methyl ester S-(2-oxo-oxazolo[4,5-b]pyridin-3-ylmethyl) ester

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / CHCl₃

2: aq. KOH / methanol / 0.08 h / Heating

With potassium hydroxide; thionyl chloride; In methanol; chloroform;
DOI:10.1002/hlca.19760590519

Reference yield:

: 16867-03-1
2-amino-3-hydroxypyridine

: 54253-87-1
ethyl-phosphonodithioic acid O-methyl ester S-(2-oxo-oxazolo[4,5-b]pyridin-3-ylmethyl) ester

Guidance literature:: Multi-step reaction with 4 steps

1: Py / 1 h / Ambient temperature

2: H₂O / 1 h

3: SOCl₂ / CHCl₃

4: aq. KOH / methanol / 0.08 h / Heating

With pyridine; potassium hydroxide; thionyl chloride; In methanol; chloroform; water;
DOI:10.1002/hlca.19760590519

Reference yield:

: 60832-72-6
2,3-dihydro[1,3]oxazolo[4,5-b]pyridin-2-one

: 54253-87-1
ethyl-phosphonodithioic acid O-methyl ester S-(2-oxo-oxazolo[4,5-b]pyridin-3-ylmethyl) ester

Guidance literature:: Multi-step reaction with 3 steps

1: H₂O / 1 h

2: SOCl₂ / CHCl₃

3: aq. KOH / methanol / 0.08 h / Heating

With potassium hydroxide; thionyl chloride; In methanol; chloroform; water;
DOI:10.1002/hlca.19760590519