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Methyl 3-amino-2,4-bis(methoxymethoxy)benzoate

Base Information
  • Chemical Name:Methyl 3-amino-2,4-bis(methoxymethoxy)benzoate
  • CAS No.:919286-02-5
  • Molecular Formula:C12H17NO6
  • Molecular Weight:271.27
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20475599
  • Nikkaji Number:J2.387.204H
  • Wikidata:Q82306229
Methyl 3-amino-2,4-bis(methoxymethoxy)benzoate

Synonyms:Methyl 3-amino-2,4-bis(methoxymethoxy)benzoate;919286-02-5;SCHEMBL15096303;DTXSID20475599

Suppliers and Price of Methyl 3-amino-2,4-bis(methoxymethoxy)benzoate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
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Chemical Property of Methyl 3-amino-2,4-bis(methoxymethoxy)benzoate
Chemical Property:
  • PSA:89.24000 
  • LogP:1.60200 
  • XLogP3:0.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:8
  • Exact Mass:271.10558726
  • Heavy Atom Count:19
  • Complexity:275
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:COCOC1=C(C(=C(C=C1)C(=O)OC)OCOC)N
Technology Process of Methyl 3-amino-2,4-bis(methoxymethoxy)benzoate

There total 7 articles about Methyl 3-amino-2,4-bis(methoxymethoxy)benzoate 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:
With hydrogen; palladium on activated charcoal; In ethyl acetate; for 16h;
DOI:10.1055/s-2007-983843
Guidance literature:
In 1,2-dichloro-benzene; at 205 ℃; for 0.0833333h; microwave irradiation;
DOI:10.1002/anie.200603892
Guidance literature:
Multi-step reaction with 5 steps
1.1: 82 percent / NaH / tetrahydrofuran / 1.5 h / 0 - 22 °C
2.1: 99 percent / H2 / Pd/C / methanol; ethyl acetate / 12 h / 22 °C
3.1: 99 percent / 4 h / 40 °C
4.1: n-BuLi; TMSCl / pentane / 0.25 h / -78 °C
4.2: n-BuLi / pentane; tetrahydrofuran / 0.5 h / -78 °C
4.3: 54 percent / aq. HCl / 0.5 h / 22 °C
5.1: 83 percent / 1,2-dichloro-benzene / 0.08 h / 205 °C / microwave irradiation
With n-butyllithium; chloro-trimethyl-silane; hydrogen; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; methanol; ethyl acetate; 1,2-dichloro-benzene; pentane;
DOI:10.1002/anie.200603892
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