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Benzyl methyl(2-(methylamino)ethyl)carbamate

Base Information
  • Chemical Name:Benzyl methyl(2-(methylamino)ethyl)carbamate
  • CAS No.:148088-78-2
  • Molecular Formula:C12H18N2O2
  • Molecular Weight:
  • Hs Code.:
  • European Community (EC) Number:866-064-4
  • DSSTox Substance ID:DTXSID90597050
  • Nikkaji Number:J1.713.883I
  • Wikidata:Q82492517
  • Mol file:148088-78-2.mol
Benzyl methyl(2-(methylamino)ethyl)carbamate

Synonyms:148088-78-2;benzyl methyl(2-(methylamino)ethyl)carbamate;Carbamic acid, N-methyl-N-[2-(methylamino)ethyl]-, phenylmethyl ester;BENZYL N-METHYL-N-[2-(METHYLAMINO)ETHYL]CARBAMATE;MFCD27979855;Benzyl methyl[2-(methylamino)ethyl]carbamate;SCHEMBL7368731;DTXSID90597050;AS-77583;DA-10080;CS-0131094;D84370;EN300-6948359;A1-48590

Suppliers and Price of Benzyl methyl(2-(methylamino)ethyl)carbamate
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
Total 4 raw suppliers
Chemical Property of Benzyl methyl(2-(methylamino)ethyl)carbamate
Chemical Property:
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:6
  • Exact Mass:222.136827821
  • Heavy Atom Count:16
  • Complexity:203
Purity/Quality:

98%min *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CNCCN(C)C(=O)OCC1=CC=CC=C1
Technology Process of Benzyl methyl(2-(methylamino)ethyl)carbamate

There total 3 articles about Benzyl methyl(2-(methylamino)ethyl)carbamate 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:
In dichloromethane; at 20 ℃; for 2h;
DOI:10.1002/anie.201916394
Guidance literature:
With hydrogenchloride; In water; acetone; at 20 ℃; for 16h;
DOI:10.3390/molecules17055346
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