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Trimethyl Orthomethoxyacetate

Base Information
  • Chemical Name:Trimethyl Orthomethoxyacetate
  • CAS No.:34359-77-8
  • Molecular Formula:C6H14O4
  • Molecular Weight:150.175
  • Hs Code.:
  • Mol file:34359-77-8.mol
Trimethyl Orthomethoxyacetate

Synonyms:Triethyl Orthomethoxyacetate;1,1,1,2-tetramethoxy-ethane;trimethyl orthoester of methoxyacetic acid;Trimethylmethoxyorthoacetat;Trimethyl Methoxyorthoacetate;

Suppliers and Price of Trimethyl Orthomethoxyacetate
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
  • Medical Isotopes, Inc.
  • TrimethylOrthomethoxyacetate
  • 1 g
  • $ 2200.00
  • Crysdot
  • 1,1,1,2-Tetramethoxyethane 97%
  • 10g
  • $ 1935.00
  • Crysdot
  • 1,1,1,2-Tetramethoxyethane 97%
  • 5g
  • $ 1340.00
  • Crysdot
  • 1,1,1,2-Tetramethoxyethane 97%
  • 1g
  • $ 644.00
Total 4 raw suppliers
Chemical Property of Trimethyl Orthomethoxyacetate
Chemical Property:
  • Vapor Pressure:5.95mmHg at 25°C 
  • Refractive Index:1.4550 (estimate) 
  • Boiling Point:146.1°C at 760 mmHg 
  • Flash Point:62.2°C 
  • PSA:36.92000 
  • Density:0.981g/cm3 
  • LogP:0.22580 
  • Storage Temp.:-20°C Freezer, Under Inert Atmosphere 
  • Solubility.:Chloroform, Methanol 
Purity/Quality:

99% *data from raw suppliers

TrimethylOrthomethoxyacetate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses Trimethyl Orthomethoxyacetate is used in Claisen rearrangements with allylic alcohols. It is also used in the preparation of oligoribonucleotides.
Technology Process of Trimethyl Orthomethoxyacetate

There total 5 articles about Trimethyl Orthomethoxyacetate 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:
Guidance literature:
at 20 ℃; for 48h;
Guidance literature:
In pentane; for 72h; Ambient temperature;
Guidance literature:
2-methoxyacetonitrile; With hydrogenchloride; In methanol; diethyl ether; at -15 - 20 ℃; for 20.33h;
methanol; In diethyl ether; for 25.5h; Heating / reflux;
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