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8-Amino-7-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylic acid ethyl ester

Base Information Edit
  • Chemical Name:8-Amino-7-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylic acid ethyl ester
  • CAS No.:30192-51-9
  • Molecular Formula:C12H11NO5
  • Molecular Weight:249.223
  • Hs Code.:
  • Mol file:30192-51-9.mol
8-Amino-7-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylic acid ethyl ester

Synonyms:8-Amino-7-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylic acid ethyl ester

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Chemical Property of 8-Amino-7-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylic acid ethyl ester Edit
Chemical Property:
  • PSA:102.76000 
  • LogP:1.83870 
Purity/Quality:
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SDS file from LookChem

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Technology Process of 8-Amino-7-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylic acid ethyl ester

There total 1 articles about 8-Amino-7-hydroxy-4-oxo-4H-1-benzopyran-2-carboxylic acid ethyl ester 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:
Aus Ethyl-7-acetoxy-8-nitro-4-oxo-4H-chromen-2-carboxylat, H2;
DOI:10.1039/j39700002518
Guidance literature:
Multi-step reaction with 5 steps
1: 92 percent / NaHCO3 / acetone / 2 h / 20 °C
2: 84 percent / ethyl polyphosphate / 1,2-dichloro-ethane / 4 h / Heating
3: 93 percent / 4 h / 140 °C
4: 66 percent / NaH; molecular sieves (4 Angstroem) / tetrahydrofuran / 20 °C
5: 59 percent / p-TsOH*H2O / CH2Cl2 / 20 h / 20 °C
With ethyl phosphate; 4 A molecular sieve; sodium hydride; sodium hydrogencarbonate; toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; 1,2-dichloro-ethane; acetone; 1: chloroacetylation / 2: Cyclization / 3: Substitution / 4: Condensation / 5: Hydrolysis;
Guidance literature:
Multi-step reaction with 5 steps
1: 92 percent / NaHCO3 / acetone / 2 h / 20 °C
2: 84 percent / ethyl polyphosphate / 1,2-dichloro-ethane / 4 h / Heating
3: 93 percent / 4 h / 140 °C
4: 60 percent / NaH; molecular sieves (4 Angstroem) / tetrahydrofuran / 20 °C
5: 60 percent / HCl (20 percent) / ethanol; tetrahydrofuran
With hydrogenchloride; ethyl phosphate; 4 A molecular sieve; sodium hydride; sodium hydrogencarbonate; In tetrahydrofuran; ethanol; 1,2-dichloro-ethane; acetone; 1: chloroacetylation / 2: Cyclization / 3: Substitution / 4: Condensation / 5: Hydrolysis;
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