(S)-Malaoxon

Base Information

Chemical Name:(S)-Malaoxon
CAS No.:145307-19-3
Molecular Formula:C₁₀H₁₉O₇PS
Molecular Weight:314.296
Hs Code.:
DSSTox Substance ID:DTXSID001019555
Nikkaji Number:J557.988K

Synonyms:(S)-Malaoxon;145307-19-3;BIDD:ER0386;CHEBI:141479;DTXSID001019555;diethyl (2S)-2-[(dimethoxyphosphoryl)thio]succinate;diethyl (2S)-2-dimethoxyphosphorylsulfanylbutanedioate;O,O-dimethyl S-[1,2-bis(ethoxycarbonyl)ethyl]thiophosphate;(2S)-2-[(Dimethoxyphosphinyl)thio]butanedioic acid, 1,4-Diethyl ester

Suppliers and Price of (S)-Malaoxon

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
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price

Total 0 raw suppliers

Chemical Property of (S)-Malaoxon

Chemical Property:

XLogP3:0.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:11
Exact Mass:314.05891111
Heavy Atom Count:19
Complexity:339

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC(=O)CC(C(=O)OCC)SP(=O)(OC)OC
Isomeric SMILES:CCOC(=O)C[C@@H](C(=O)OCC)SP(=O)(OC)OC

Technology Process of (S)-Malaoxon

There total 4 articles about (S)-Malaoxon 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:

: 121-75-5
[(dimethoxyphosphinothioyl)thio]-butanedioic acid, diethyl ester

: 1634-78-2,35805-20-0,145307-18-2,145307-19-3
malaoxon

Guidance literature:: With nitric acid;

Reference yield:

: 23060-14-2
diethyl 2-mercaptosuccinate

: 1634-78-2,35805-20-0,145307-18-2,145307-19-3
malaoxon

Guidance literature:: Multi-step reaction with 2 steps

1: aq. I₂, KI

2: 2 h / 110 - 115 °C

With iodine; potassium iodide;
DOI:10.1021/jo01015a028