Glycine, N-(2-quinoxaloyl)-

Base Information

Chemical Name:Glycine, N-(2-quinoxaloyl)-
CAS No.:5569-99-3
Molecular Formula:C11H9N3O3
Molecular Weight:231.2075
Hs Code.:
NSC Number:70625
DSSTox Substance ID:DTXSID80204221
Nikkaji Number:J49.233G
Wikidata:Q83077671
Mol file:5569-99-3.mol

Synonyms:5569-99-3;GLYCINE, N-(2-QUINOXALOYL)-;N-(2-Quinoxaloyl)-glycine;Glycine, N-(2-quinoxalinylcarbonyl)-;2-(quinoxaline-2-carbonylamino)acetic acid;2-(Quinoxaline-2-carboxamido)acetic acid;NSC 70625;BRN 0533185;Glycine, N-(2-quinoxalinylcarbonyl)- (9CI);5-25-04-00347 (Beilstein Handbook Reference);C11H9N3O3;WLN: T66 BN ENJ CVM1VQ;NSC70625;DTXSID80204221;N-(Quinoxalin-2-ylcarbonyl)glycine;NSC-70625;AKOS005068104;LS-72872;[(2-quinoxalinylcarbonyl)amino]acetic acid;2-[(quinoxalin-2-yl)formamido]acetic acid;AE-641/40198076

Suppliers and Price of Glycine, N-(2-quinoxaloyl)-

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

American Custom Chemicals Corporation
2-(QUINOXALIN-2-YLFORMAMIDO)ACETIC ACID 95.00%
5MG
$ 498.66

Total 4 raw suppliers

Chemical Property of Glycine, N-(2-quinoxaloyl)-

Chemical Property:

Vapor Pressure:1.35E-14mmHg at 25°C
Boiling Point:586.4°Cat760mmHg
Flash Point:308.5°C
PSA：92.18000
Density:1.431g/cm³
LogP:0.83510
XLogP3:1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:231.06439116
Heavy Atom Count:17
Complexity:308

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

2-(QUINOXALIN-2-YLFORMAMIDO)ACETIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)N=CC(=N2)C(=O)NCC(=O)O

Technology Process of Glycine, N-(2-quinoxaloyl)-

There total 3 articles about Glycine, N-(2-quinoxaloyl)- 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: 84.0%

: 93003-54-4
N-(quinoxaline-2-carbonyl)-glycine ethyl ester

: 5569-99-3
N--glycin

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 0.5h; Inert atmosphere;
DOI:10.1021/acs.jmedchem.9b02039

Reference yield:

: 879-65-2
quinoxaline-2-carboxylic acid

: 5569-99-3
N--glycin

Guidance literature:: Multi-step reaction with 2 steps

1: 4-methyl-morpholine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methoxymorpholinium chloride / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

2: sodium hydroxide / water; tetrahydrofuran / 0.5 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methoxymorpholinium chloride; sodium hydroxide; In tetrahydrofuran; water; N,N-dimethyl-formamide;
DOI:10.1021/acs.jmedchem.9b02039