Ethyl 2-hydroxy-3-(2-quinoxalinyl)propanoate

Base Information

• Chemical Name: Ethyl 2-hydroxy-3-(2-quinoxalinyl)propanoate
• CAS No.: 6639-94-7
• Molecular Formula: C13H14N2O3
• Molecular Weight: 246.2619
• NSC Number: 48961
• DSSTox Substance ID: DTXSID50287107
• Nikkaji Number: J3.322.783C
• ChEMBL ID: CHEMBL1986744
• Mol file: 6639-94-7.mol

Synonyms:6639-94-7;ethyl 2-hydroxy-3-(2-quinoxalinyl)propanoate;NSC48961;ETHYL 2-HYDROXY-3-(QUINOXALIN-2-YL)PROPANOATE;NSC-48961;CHEMBL1986744;SCHEMBL15599302;DTXSID50287107;NCI60_004176

Chemical Property of Ethyl 2-hydroxy-3-(2-quinoxalinyl)propanoate

Chemical Property:

• Vapor Pressure: 7.48E-07mmHg at 25°C
• Boiling Point: 392.1°C at 760 mmHg
• Flash Point: 191°C
• Density: 1.271g/cm³
• XLogP3: 1.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 5
• Exact Mass: 246.10044231
• Heavy Atom Count: 18
• Complexity: 285

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC(=O)C(CC1=NC2=CC=CC=C2N=C1)O

Technology Process of Ethyl 2-hydroxy-3-(2-quinoxalinyl)propanoate

There total 1 articles about Ethyl 2-hydroxy-3-(2-quinoxalinyl)propanoate 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:

Reference yield: 88.0%

2-methylquinoxaline (7251-61-8) + glyoxylic acid ethyl ester (924-44-7) → ethyl 2-hydroxy-3-(quinoxalin-2-yl)propanoate (6639-94-7)

Guidance literature:

With iron(II) acetate; In 1,4-dioxane; at 120 ℃; for 24h; Inert atmosphere; Schlenk technique; Green chemistry;

DOI:10.1039/c4ra10939b

upstream raw materials:

2-methylquinoxaline

glyoxylic acid ethyl ester