21911-61-5

Basic information

• Product Name: 2-[methyl(phenyl)amino]acetic acid
• Synonyms: 2-[methyl(phenyl)amino]acetic acid;Albb-003985;N-(2-methylphenyl)glycine(SALTDATA: FREE);N-(2-Methylphenyl)glycine
• CAS NO: 21911-61-5
• Molecular Formula: C₉H₁₁NO₂
• Molecular Weight: 165.19
• Mol File: 21911-61-5.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 366.6°C at 760 mmHg
• Flash Point: 175.5°C
• Appearance: /
• Density: 1.211g/cm³
• Vapor Pressure: 5.1E-06mmHg at 25°C
• Refractive Index: 1.604
• CAS DataBase Reference: 2-[methyl(phenyl)amino]acetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[methyl(phenyl)amino]acetic acid(21911-61-5)
• EPA Substance Registry System: 2-[methyl(phenyl)amino]acetic acid(21911-61-5)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 21911-61-5(Hazardous Substances Data)

Usage

General Description

"2-[methyl(phenyl)amino]acetic acid" is a chemical compound that is categorized as an organonitrogen compound and is primarily composed of carbon, hydrogen, nitrogen, and oxygen atoms. This chemical structure consists of an acetic acid moiety attached to a methyl-phenyl amine group. Its molecular formula is C9H11NO2 and its exact mass is 165.07898 g/mol. As with many chemicals, it should be handled with care as it may pose potential health risks. Due to its unique structure, this compound may serve as a building block in the synthesis of various organic compounds and can be used in various applications in the field of chemistry and biochemistry. However, specific details about its uses are not broadly documented in the literature and may be restricted to specialized chemical research.

InChI:InChI=1/C9H11NO2/c1-7-4-2-3-5-8(7)10-6-9(11)12/h2-5,10H,6H2,1H3,(H,11,12)

Upstream product

• 79-11-8 chloroacetic acid 
• 95-53-4 o-toluidine 
• 7732-18-5 water 
• 127-09-3 sodium acetate 
• 598-21-0 2-Bromoacetyl bromide 
• 69825-49-6 N-(2-methylphenyl)glycine ethyl ester 
• 105-36-2 ethyl bromoacetate 
• 7647-01-0 hydrogenchloride 
• 74-87-3 methylene chloride 
• 3926-62-3 sodium monochloroacetic acid 
• 88-72-2 1-methyl-2-nitrobenzene 

Downstream Products

• 69825-49-6 N-(2-methylphenyl)glycine ethyl ester 
• 64450-25-5 4-[(2-methylphenyl)amino]butan-2-one 
• 5405-13-0 N-benzyl-2-methylaniline 
• 183014-07-5 ethyl 1-(2-methylphenyl)-aziridine-2-carboxylate 
• 87565-00-2 C₁₈H₂₀CuN₂O₄ 
• 21074-17-9 4-bromo-3-o-tolylsydnone 
• 3483-18-9 3-o-tolyl-sydnone 
• 2563-89-5 N-o-tolyl-glycine o-toluidide 

Relevant articles and documents

Perovskite as Recyclable Photocatalyst for Annulation Reaction of N-Sulfonyl Ketimines

A sustainable and cost-effective manner for the photocatalytic annulation reaction of N-sulfonyl ketimines with N-arylglycines to synthesize imidazolidine-fused sulfamidates (31 examples) by employing CsPbBr3 as a heterogeneous photocatalyst has been developed. The catalyst CsPbBr3 can be simply recovered from the reaction mixture and reused at least five times without an obvious reduction in its photocatalytic reactivity, exhibiting a high catalyst economic feature.

Synthesis and evaluation of phenyl substituted sydnones as potential DPPH-radical scavengers

A series of phenyl substituted sydnones has been synthesized and their radical-scavenging activity has been studied on DPPH free radical. Out of eighteen compounds screened, nine compounds show interesting activity. A mechanism is presented whereby sydnones scavenge DPPH radical through donating H-atom at 4th-position. Its strong radical-scavenging activity mainly arises from 1, 2, 3-oxadiazolium-5-olate ring. Different substituents and their positions on the phenyl ring differently influence DPPH scavenging activity and therefore, may provide clues to design and develop better free-radical scavenging sydnones with multiple activities.

Soluble Polymer-Supported Synthesis of α-Amino Acid Derivatives

A practical and efficient synthesis of N-substituted α-amino acid derivatives on soluble polymer support is described.