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2-diethoxyphosphoryl-N-methoxy-N-methylacetamide

Base Information Edit
  • Chemical Name:2-diethoxyphosphoryl-N-methoxy-N-methylacetamide
  • CAS No.:124931-12-0
  • Molecular Formula:C8H18 N O5 P
  • Molecular Weight:239.208
  • Hs Code.:29319000
  • European Community (EC) Number:626-937-0
  • DSSTox Substance ID:DTXSID70378667
  • Nikkaji Number:J860.320K
  • Wikidata:Q82168183
  • Mol file:124931-12-0.mol
2-diethoxyphosphoryl-N-methoxy-N-methylacetamide

Synonyms:124931-12-0;Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonate;2-diethoxyphosphoryl-N-methoxy-N-methylacetamide;Diethyl (2-(methoxy(methyl)amino)-2-oxoethyl)phosphonate;Diethyl(N-methoxy-N-methylcarbamoylmethyl)phosphonate;Diethyl N-methoxy-N-methylphosphonoacetamide;2-diethoxyphosphoryl-N-methoxy-N-methyl-acetamide;diethyl {[methoxy(methyl)carbamoyl]methyl}phosphonate;diethyl {2-[methoxy(methyl)amino]-2-oxoethyl}phosphonate;SBB057815;diethyl (n-methoxy-n-methylcarbamoyl-methyl)phosphonate;SCHEMBL224985;DTXSID70378667;WYLRYBDGIILFIR-UHFFFAOYSA-N;(N-Methoxy-N-methylcarbamoylmethyl)phosphonic Acid Diethyl Ester;ZEA93112;BBL102956;MFCD00134233;STL556765;AKOS015916081;AM803081;N-methoxy-N-methyl diethylphosphonoacetamide;CS-0037993;D3708;N-methoxy-N-methyl diethylphosphonoacetarnide;N-Methoxy-N-methyldiethoxyphosphinylacetamide;EN300-7415618;A890344;N-Methoxy-N-methyl-2-(diethyl phosphono)acetamide;J-005180;N-Methoxy-N-methyl-phosphonoacetamide diethyl ester;diethyl 2-(methoxy(methyl)amino)-2-oxoethylphosphonate;diethyl(N-methoxy-N-methyl-carbamoylmethyl)phosphonate;diethyl-(N-methoxy-N-methyl-carbamoylmethyl)-phosphonate;Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonate, 96%

Suppliers and Price of 2-diethoxyphosphoryl-N-methoxy-N-methylacetamide
Supply Marketing:Edit
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
  • Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonate
  • 500mg
  • $ 110.00
  • TRC
  • Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonate
  • 100mg
  • $ 60.00
  • TCI Chemical
  • Diethyl (N-Methoxy-N-methylcarbamoylmethyl)phosphonate >97.0%(GC)
  • 1g
  • $ 34.00
  • TCI Chemical
  • Diethyl (N-Methoxy-N-methylcarbamoylmethyl)phosphonate >97.0%(GC)
  • 5g
  • $ 102.00
  • Sigma-Aldrich
  • Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonate 96%
  • 5g
  • $ 298.00
  • Crysdot
  • Diethyl(2-(methoxy(methyl)amino)-2-oxoethyl)phosphonate 95+%
  • 10g
  • $ 349.00
  • ChemScene
  • Diethyl(2-(methoxy(methyl)amino)-2-oxoethyl)phosphonate ≥97.0%
  • 5g
  • $ 231.00
  • ChemScene
  • Diethyl(2-(methoxy(methyl)amino)-2-oxoethyl)phosphonate ≥97.0%
  • 1g
  • $ 77.00
  • American Custom Chemicals Corporation
  • Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonate 95.00%
  • 1G
  • $ 441.40
  • American Custom Chemicals Corporation
  • Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonate 95.00%
  • 5G
  • $ 607.00
Total 13 raw suppliers
Chemical Property of 2-diethoxyphosphoryl-N-methoxy-N-methylacetamide Edit
Chemical Property:
  • Vapor Pressure:0.00135mmHg at 25°C 
  • Refractive Index:n20/D 1.455(lit.) 
  • Boiling Point:297.4°Cat760mmHg 
  • Flash Point:133.7°C 
  • PSA:74.88000 
  • Density:1.148g/cm3 
  • LogP:1.27230 
  • XLogP3:-0.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:7
  • Exact Mass:239.09225967
  • Heavy Atom Count:15
  • Complexity:235
Purity/Quality:

98%,99%, *data from raw suppliers

Diethyl (N-methoxy-N-methylcarbamoylmethyl)phosphonate *data from reagent suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCOP(=O)(CC(=O)N(C)OC)OCC
  • Uses Reactant for:Preparation of ring-expanded bryostatin analogs as antitumor agentsAsymmertic synthesis of pinnatoxins A and G via diastereoselective Ireland-Claisen rearrangement, ring closing metathesis, and cyclizationRh2(II)-catalyzed nitro-group migration reactionsStereoselective synthesis of cyclohexanones via phase transfer catalyzed double addition reactionsStereoselective synthesis of (+)-polyrhacitide A via aldol reaction, Horner-Wardsworth-Emmons reaction, Evans acetal intramolecular oxa-Michael reaction and diastereoselective syn reduction reaction as the key stepsPreparation of substituted furans via olefin cross-metathesis
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