24539-99-9

Basic information

• Product Name: 2-phenyl-2-phthalimidopropionic acid
• CAS NO: 24539-99-9
• Molecular Weight: 295.295
• Mol File: 24539-99-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-phenyl-2-phthalimidopropionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenyl-2-phthalimidopropionic acid(24539-99-9)
• EPA Substance Registry System: 2-phenyl-2-phthalimidopropionic acid(24539-99-9)

Safety Data

• Hazardous Substances Data: 24539-99-9(Hazardous Substances Data)

Upstream product

• 6843-49-8 5-methyl-5-phenylimidazolidin-2,4-dione 
• 85-44-9 phthalic anhydride 
• 565-07-1 2-amino-2-phenylpropanoic acid 

Downstream Products

• 24540-00-9 2-methyl-2-phthalimidophenylacetyl chloride 
• 16707-52-1 (+/-)-3-Amino-3-phenyl-2-butanon 

Relevant articles and documents

Aminotetralone Analogues of Ketamine: Synthesis and Evaluation of Hypnotic and Locomotor Properties in Mice

Ketamine and phencyclidine are structurally similar compounds that share many pharmacological actions, some of which are similar to the phenethylamines amphetamine and cathione.In order to integrate structural features of ketamine and cathinone, two groups of analogues, which are more conformationally restricted compared to the parent compounds, were synthesized for biological evaluation.These included 1-amino-1-methyl-2-tetralone and 2-amino-2-methyl-1-tetralone was well as several N-substituted derivatives of these molecules.Locomotor activity testing in mice revealed that 2-amino-2-methyl-1-tetralone caused an increase in locomotor activity while 1-amino-1-methyl-2-tetralone depressed soontaneous locomotor activity.None of the compounds produced hypnosis or profound ataxia.

Dihydroimidaz oisoindolediones and the use thereof as herbicidal agents

The invention relates to novel dihydroimidazoisoindoledione compounds and the optical and stereo isomers thereof. This invention also relates to a method for the control of undesirable plant species with the dihydroimidazoisoindolediones and their optical and stereo isomers, and further, to a process for the preparation of the compounds.