[(2,4-Dioxoimidazolidin-1-yl)imino]acetic acid

Base Information

• Chemical Name: [(2,4-Dioxoimidazolidin-1-yl)imino]acetic acid
• CAS No.: 64748-89-6
• Molecular Formula: C5H5N3O4
• Molecular Weight: 171.1109
• DSSTox Substance ID: DTXSID80700718

Synonyms:2-[(2,4-DIOXO-1-IMIDAZOLIDINYL)IMINO]ACETIC ACID;SCHEMBL11735291;DTXSID80700718;FT-0667633;[(2,4-Dioxoimidazolidin-1-yl)imino]acetic acid

Chemical Property of [(2,4-Dioxoimidazolidin-1-yl)imino]acetic acid

Chemical Property:

• PSA: 102.56000
• LogP: -1.17760
• Storage Temp.: Refrigerator
• Solubility.: Acetonitrile (Slightly, Heated), DMSO (Slightly)
• XLogP3: -0.9
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2
• Exact Mass: 171.02800565
• Heavy Atom Count: 12
• Complexity: 272

Purity/Quality:

98% ^*data from raw suppliers

2-[(2,4-Dioxo-1-imidazolidinyl)imino]aceticAcid ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1C(=O)NC(=O)N1N=CC(=O)O
• Uses: Azumolene intermediate.

Technology Process of [(2,4-Dioxoimidazolidin-1-yl)imino]acetic acid

There total 2 articles about [(2,4-Dioxoimidazolidin-1-yl)imino]acetic acid 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: 73.0%

1-aminohydantoin hydrochloride (2827-56-7) + Glyoxilic acid (298-12-4) → <<(2,4-dioxo-1-imidazolidinyl)imino>methyl>formic acid (64748-89-6)

Guidance literature:

In water;

DOI:10.1021/jm00385a006

Reference yield:

→ <<(2,4-dioxo-1-imidazolidinyl)imino>methyl>formic acid (64748-89-6)

Guidance literature:

aus Glyoxylsaeure m. Aminohydantoin;

Reference yield:

<<(2,4-dioxo-1-imidazolidinyl)imino>methyl>formic acid (64748-89-6) → 2-[(Z)-2,4-Dioxo-imidazolidin-1-ylimino]-N-[2-(2-nitro-phenyl)-2-oxo-ethyl]-acetamide (105336-07-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 60 percent / SOCl₂ / dioxane / 5 h / Heating

2: 50 percent / pyridine / dimethylformamide

With pyridine; thionyl chloride; In 1,4-dioxane; N,N-dimethyl-formamide;

DOI:10.1021/jm00385a006

upstream raw materials:

1-aminohydantoin hydrochloride

Glyoxilic acid

Downstream raw materials:

1-{[1-[5-(4-Methoxy-phenyl)-oxazol-2-yl]-meth-(E)-ylidene]-amino}-imidazolidine-2,4-dione

N-[2-(3-Chloro-phenyl)-2-oxo-ethyl]-2-[(Z)-2,4-dioxo-imidazolidin-1-ylimino]-acetamide

N-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-2-[(Z)-2,4-dioxo-imidazolidin-1-ylimino]-acetamide

1-{[1-[5-(2-Nitro-phenyl)-oxazol-2-yl]-meth-(Z)-ylidene]-amino}-imidazolidine-2,4-dione

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