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Ethyl 2-amino-1-(2,5-dimethoxyphenyl)pyrrolo[3,2-b]quinoxaline-3-carboxylate

Base Information
  • Chemical Name:Ethyl 2-amino-1-(2,5-dimethoxyphenyl)pyrrolo[3,2-b]quinoxaline-3-carboxylate
  • CAS No.:4622-69-9
  • Molecular Formula:C10H16N5O13P3
  • Molecular Weight:508.21
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20365603
  • Wikidata:Q82150394
Ethyl 2-amino-1-(2,5-dimethoxyphenyl)pyrrolo[3,2-b]quinoxaline-3-carboxylate

Synonyms:ethyl 2-amino-1-(2,5-dimethoxyphenyl)pyrrolo[3,2-b]quinoxaline-3-carboxylate;326924-46-3;4622-69-9;Oprea1_226310;Oprea1_824765;DTXSID20365603;STK530515;AKOS001010637;AB00709553-01;SR-01000028721;SR-01000028721-1;Z56787072;ethyl 2-amino-1-(2,5-dimethoxyphenyl)-1H-pyrrolo[2,3-b]quinoxaline-3-carboxylate

Suppliers and Price of Ethyl 2-amino-1-(2,5-dimethoxyphenyl)pyrrolo[3,2-b]quinoxaline-3-carboxylate
Supply Marketing:
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Ethyl 2-amino-1-(2,5-dimethoxyphenyl)pyrrolo[3,2-b]quinoxaline-3-carboxylate
Chemical Property:
  • Vapor Pressure:7.65E-13mmHg at 25°C 
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:6
  • Exact Mass:392.14845513
  • Heavy Atom Count:29
  • Complexity:579
Purity/Quality:
Safty Information:
  • Pictogram(s):  
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MSDS Files:
Useful:
  • Canonical SMILES:CCOC(=O)C1=C(N(C2=NC3=CC=CC=C3N=C12)C4=C(C=CC(=C4)OC)OC)N
Technology Process of Ethyl 2-amino-1-(2,5-dimethoxyphenyl)pyrrolo[3,2-b]quinoxaline-3-carboxylate

There total 2 articles about Ethyl 2-amino-1-(2,5-dimethoxyphenyl)pyrrolo[3,2-b]quinoxaline-3-carboxylate 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 piruvate kinase; T5 bacteriophage deoxynucleoside monophosphate kinase; potassium chloride; dATP; magnesium chloride; diothiothreitol; at 37 ℃; for 0.5h; pH=8; Tris-HCl buffer; Enzymatic reaction;
DOI:10.1134/S1068162009060090
Guidance literature:
32P-Adenosin-5'-monophosphat, 1.)->32P-Adenosin-5'-morpholinophosphat, 2.)Pyrophosphat, wasserfr.DMSO;
DOI:10.1021/ja01060a066
upstream raw materials:

[32P]-adenosine-5'-phosphate

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