ETHYL UREIDOACETATE

Base Information

• Chemical Name: ETHYL UREIDOACETATE
• CAS No.: 6293-20-5
• Molecular Formula: C5H10 N2 O3
• Molecular Weight: 146.146
• Hs Code.: 2924199090
• Mol file: 6293-20-5.mol

Synonyms:Glycine,N-carbamoyl-, ethyl ester (7CI,8CI); Hydantoic acid, ethyl ester (6CI);N-Carbamoylglycine ethyl ester; N-Ethoxycarbonylmethylurea; NSC 8846

Chemical Property of ETHYL UREIDOACETATE

Chemical Property:

• Melting Point: 146-148°
• PSA: 81.42000
• LogP: 0.30900

Purity/Quality:

98%min ^*data from raw suppliers

HydantoicAcidEthylEster ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

• Uses: Hydantoic Acid Ethyl Ester is useful for the preparation of benzoylhydantoic acids by reaction with benzoic acids.

Technology Process of ETHYL UREIDOACETATE

There total 8 articles about ETHYL UREIDOACETATE 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: 90.0%

potassium cyanate (590-28-3) + glycine ethyl ester hydrochloride (623-33-6) → ethyl hydantoate (6293-20-5)

Guidance literature:

In water;

Reference yield: 80.0%

Glycine ethyl ester isocyanate (2949-22-6) → ethyl hydantoate (6293-20-5)

Guidance literature:

With ammonia; In diethyl ether; isopropyl alcohol; at 0 - 20 ℃; for 1h;

DOI:10.1016/j.tetlet.2016.04.039

Reference yield: 70.0%

glycine ethyl ester hydrochloride (623-33-6) + urea (57-13-6) → ethyl hydantoate (6293-20-5)

Guidance literature:

In water; for 5h; Heating;

DOI:10.1021/jm9508393

upstream raw materials:

ethanol

N-carbamoylglycine

potassium cyanate

glycine ethyl ester hydrochloride

Downstream raw materials:

ethyl 2,4,5-trioxoimidazolidine-1-acetate

N-ethoxycarbonylmethylbarbituric acid

2,4-imidazolidinedione

3-nitroso-hydantoic acid ethyl ester

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