58942-04-4

Basic information

• Product Name: 5-[(4-hydroxyphenyl)methyl]imidazolidine-2,4-dione
• Synonyms: 5-[(4-hydroxyphenyl)methyl]imidazolidine-2,4-dione;Nsc56834
• CAS NO: 58942-04-4
• Molecular Formula: C₁₀H₁₀N₂O₃
• Molecular Weight: 206.2
• Mol File: 58942-04-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 340.2°C at 760 mmHg
• Flash Point: 159.6°C
• Appearance: /
• Density: 1.041g/cm³
• Vapor Pressure: 8.71E-05mmHg at 25°C
• Refractive Index: 1.512
• CAS DataBase Reference: 5-[(4-hydroxyphenyl)methyl]imidazolidine-2,4-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 5-[(4-hydroxyphenyl)methyl]imidazolidine-2,4-dione(58942-04-4)
• EPA Substance Registry System: 5-[(4-hydroxyphenyl)methyl]imidazolidine-2,4-dione(58942-04-4)

Safety Data

• Hazardous Substances Data: 58942-04-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H13NO/c1-12(10-14,8-5-9-13)11-6-3-2-4-7-11/h2-4,6-7,10H,5,8H2,1H3

Upstream product

• 80171-33-1 5-(p-hydroxybenzylidene)hydantoin 
• 590-28-3 potassium cyanate 
• 556-02-5 ?Tyr 
• 6318-40-7 (5Z)-5-(4-hydroxybenzylidene)-2-thioxoimidazolidin-4-one 
• 80171-33-1 5-(4-hydroxybenzylidene)imidazolidine-2,4-dione 
• 57-13-6 urea 
• 54896-65-0 N-carbamoyltyrosine 
• 123-08-0 4-hydroxy-benzaldehyde 

Downstream Products

• 90899-85-7 N-carbamoyl-L-tyrosine 
• 54896-58-1 N-carbamyl-D-tyrosine 
• 7664-41-7 ammonia 
• 556-02-5 ?Tyr 
• 15719-64-9 methylammonium carbonate 
• 54896-65-0 N-carbamoyltyrosine 

Relevant articles and documents

Method for preparing 5-substituted chiral hydantoin

The invention discloses a method for directly preparing a 5-substituted chiral hydantoin compound by asymmetric catalyzing and hydrogenating of hydantoin-derived exocycloolefin. A chemical structural formula of the 5-substituted chiral hydantoin compound is expressed by a formula (I) shown in the description. A chemical reaction equation is shown in the description, wherein a compound (II) is the hydantoin-derived exocycloolefin; a compound (III) is a catalyst, and the catalyst is a metal compound of chiral diphosphine ligand. Compared with the prior art, the method has the characteristics that the chiral multiplication is realized, the efficiency and selectivity are high, the atom economy is realized, the green and non-pollution effects are realized, the industrialization is easy, and the like.