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N-(Methoxymethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine

Base Information
  • Chemical Name:N-(Methoxymethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine
  • CAS No.:88211-44-3
  • Molecular Formula:C8H23 N O Si2
  • Molecular Weight:205.448
  • Hs Code.:2931900090
  • DSSTox Substance ID:DTXSID80463351
  • Nikkaji Number:J1.202.876H
  • Wikidata:Q82288212
  • Mol file:88211-44-3.mol
N-(Methoxymethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine

Synonyms:88211-44-3;N-(Methoxymethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine;1-methoxy-N,N-bis(trimethylsilyl)methanamine;SCHEMBL4907600;DTXSID80463351;MFCD17018871;SY287544;N,N-bis(trimethylsilyl)aminomethyl methyl ether

Suppliers and Price of N-(Methoxymethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine
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
  • American Custom Chemicals Corporation
  • AMINOMETHYLATING REAGENT A 95.00%
  • 5MG
  • $ 496.50
Total 3 raw suppliers
Chemical Property of N-(Methoxymethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine
Chemical Property:
  • Boiling Point:73 °C(Press: 16 Torr) 
  • PKA:11.16±0.70(Predicted) 
  • PSA:12.47000 
  • Density:0.836±0.06 g/cm3(Predicted) 
  • LogP:2.56210 
  • Solubility.:sol organic solvents such as hexane, dichloromethane, ether, alcohol; stable in neutral or basic solvents; unstable in protic solvents. 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:205.13181743
  • Heavy Atom Count:12
  • Complexity:123
Purity/Quality:

AMINOMETHYLATING REAGENT A 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:COCN([Si](C)(C)C)[Si](C)(C)C
  • Physical properties bp 94–95 °C/83 mmHg; d 0.873 g cm?3; n20 D 1.431–1.434.
  • Uses (Methoxymethyl)bis(trimethylsilyl)amine is widely used as electrophilic N,N-bis(trimethylsilyl)aminomethylating agent for a variety of molecules; after desilylation, the overall transformation achieves primary aminomethylation.
Technology Process of N-(Methoxymethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine

There total 4 articles about N-(Methoxymethyl)-1,1,1-trimethyl-N-(trimethylsilyl)silanamine 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:
1,1,1,3,3,3-hexamethyl-disilazane; With n-butyllithium; In tetrahydrofuran; at 0 ℃; for 0.5h; Inert atmosphere;
chloromethyl methyl ether; In tetrahydrofuran; at 0 ℃; for 2h; Inert atmosphere;
DOI:10.1021/jacs.1c00249
Guidance literature:
In tetrahydrofuran; for 36h; Ambient temperature;
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