62044-15-9

Basic information

• Product Name: 4-AMINOPHENYLACETONE
• Synonyms: 1-(4-aminophenyl)propan-2-one
• CAS NO: 62044-15-9
• Molecular Formula: C₉H₁₁NO
• Molecular Weight: 149.19
• Product Categories: Aromatic Ketones (substituted)
• Mol File: 62044-15-9.mol
• Article Data: 9

Chemical Properties

• Melting Point: 99-100 °C
• Boiling Point: 275.2±15.0 °C(Predicted)
• Appearance: /
• Density: 1.079±0.06 g/cm3(Predicted)
• PKA: 4.58±0.10(Predicted)
• CAS DataBase Reference: 4-AMINOPHENYLACETONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-AMINOPHENYLACETONE(62044-15-9)
• EPA Substance Registry System: 4-AMINOPHENYLACETONE(62044-15-9)

Safety Data

• Hazardous Substances Data: 62044-15-9(Hazardous Substances Data)

Upstream product

• 104-03-0 4-nitrobenzeneacetic acid 
• 4231-16-7 1-(p-nitrophenyl)-2-nitro-1-propene 
• 29865-60-9 1-nitro-4-(2-nitropropyl)benzene 
• 1197-55-3 4-aminophenylacetic acid 
• 108-24-7 acetic anhydride 
• 5332-96-7 1-(4-nitrophenyl)propan-2-one 
• 74701-66-9 1-(prop-1-en-2-yl)pyrrolidine 
• 106-47-8 4-chloro-aniline 
• 3369-75-3 2-(triethylsilyloxy)propene 

Downstream Products

• 217808-43-0 (R)-4-(2-(methyl(prop-2-yn-1-yl)amino)propyl)aniline 
• 887624-89-7 2,2,2-Trichloroethyl [4-(2-oxopropyl)phenyl}carbamate 
• 1357589-43-5 1-(4-amino-3-chlorophenyl)propan-2-one 

Relevant articles and documents

PESTICIDAL COMPOSITIONS AND METHODS

This disclosure relates to the field of molecules having pesticidal utility against pests in phyla Nematoda, Arthropoda, and/or Mollusca, processes to produce such molecules and intermediates used in such processes, compositions containing such molecules, and processes of using such molecules against such pests. These molecules may be used, for example, as nematicides, acaricides, insecticides, miticides, and/or molluscicides. This document discloses molecules having the structure of Formula A.

HETEROARYL INHIBITORS OF PDE4

The present invention relates to compounds and methods useful as inhibitors of phosphodiesterase 4 (PDE4) for the treatment or prevention of disease.

General and selective iron-catalyzed transfer hydrogenation of nitroarenes without base

The first well-defined iron-based catalyst system for the reduction of nitroarenes to anilines has been developed applying formic acid as reducing agent. A broad range of substrates including other reducible functional groups were converted to the corresponding anilines in good to excellent yields at mild conditions. Notably, the process constitutes a rare example of base-free transfer hydrogenations.