1012-87-9

Basic information

• Product Name: 2,4-Oxazolidinedione, 5-methyl-3-phenyl-
• CAS NO: 1012-87-9
• Molecular Formula: C10H9NO3
• Molecular Weight: 191.186
• Mol File: 1012-87-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,4-Oxazolidinedione, 5-methyl-3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-Oxazolidinedione, 5-methyl-3-phenyl-(1012-87-9)
• EPA Substance Registry System: 2,4-Oxazolidinedione, 5-methyl-3-phenyl-(1012-87-9)

Safety Data

• Hazardous Substances Data: 1012-87-9(Hazardous Substances Data)

Usage

Physical form

white crystalline powder

Odor

faint

Primary use

intermediate in the synthesis of various pharmaceuticals

Pharmacological properties

anticonvulsant, hypoglycemic, xanthine oxidase inhibition activities

Importance

important compound for the development of new drugs and treatments for various medical conditions

Safety precautions

potential health hazards require proper handling and use

Upstream product

• 73622-98-7 (-)-2-phenylcarbamoyloxy-propionic acid 
• 7732-18-5 water 
• 52569-43-4 5-methyl-4-methylene-N-phenyl-2-oxazolidinone 
• 103-71-9 phenyl isocyanate 
• 106942-22-7 lactanilide 
• 849585-22-4 LACTIC ACID 
• 547-64-8 methyl lactate 
• 103-72-0 phenyl isothiocyanate 
• 17578-13-1 5-methyl-1,3-dioxolane-2,4-dione 
• 97-64-3 ethyl 2-hydroxypropionate 
• 108906-58-7 2-phenylcarbamoyloxy-propionic acid anilide 

Downstream Products

• 1234623-29-0 C₁₇H₁₅NO₃ 
• 1234623-28-9 C₁₃H₁₃NO₃ 
• 1234623-13-2 C₁₂H₁₅NO₂ 
• 1234623-30-3 C₁₅H₁₇NO₃ 
• 107940-25-0 5-Methyl-3-phenyl-4-(trimethylsiloxy)-4-oxazol-2(3H)-on 

Relevant articles and documents

Versatile synthesis of quaternary 1,3-oxazolidine-2,4-diones and their use in the preparation of α-hydroxyamides

A new approach to the synthesis of 1,3-oxazolidine-2,4-diones, via a two-step reaction sequence, starting from the readily available α-ketols and isocyanates, is reported. The condensation of the latter led to the key precursors 4-methylene-2-oxazolidinon

Silver(I) ion-mediated desulfurization-cyclization of isothiocyanates with several hydroxy acids and N-substituted amino acids

The title reaction of 2-hydroxy-2-methylpropionic acid with phenyl isothiocyanate gave 5,5-dimethyl-3-phenyl-2,4-oxazolidinedione. The structure was determined by X-Ray crystal analysis, and the reaction pathway was estimated. The reactions of other 2-hyd