64790-08-5

Basic information

• Product Name: Acetamide, N-(2-oxoethyl)-
• Synonyms: 2-acetamidoacetaldehyde;Acetamidoacetaldehyde;N-acetamidoacetaldehyde;Acetylamino-acetaldehyd;N-acetylaminoacetaldehyde
• CAS NO: 64790-08-5
• Molecular Formula: C4H7NO2
• Molecular Weight: 101.105
• Mol File: 64790-08-5.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 280.8±23.0 °C(Predicted)
• Density: 1.033±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Acetamide, N-(2-oxoethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-(2-oxoethyl)-(64790-08-5)
• EPA Substance Registry System: Acetamide, N-(2-oxoethyl)-(64790-08-5)

Safety Data

• Hazardous Substances Data: 64790-08-5(Hazardous Substances Data)

Upstream product

• 62005-48-5 N-acetylaminoacetaldehyde dimethyl acetal 
• 120990-24-1 (E)-3-Acetamido-1-phenylprop-1-ene 
• 692-33-1 N-allylacetamide 
• 142-26-7 2-acetylaminoethanol 
• 85483-61-0 acetamido acetaldehyde diethyl acetal 

Relevant articles and documents

-

-

LSD1 INHIBITORS AND MEDICAL USES THEREOF

Provided are novel compounds of Formula (I or Ia'): and pharmaceutically acceptable salts thereof, which are useful for treating a variety of diseases, disorders or conditions, associated with LSD1. Also provided are pharmaceutical compositions comprising

Synthesis of Analogues of 1,3-Dihydroxyacetone Phosphate and Glyceraldehyde 3-Phosphate for Use in Studies of Fructose-1,6-diphosphate Aldolase

This paper describes the synthesis of five analogues of dihydroxyacetone phosphate (3-azidohydroxyacetone 1-phosphate (5), 3-(acetylamino)hydroxyacetone 1-phosphate (12), (R)-1,3-dihydroxy-2-butanone 1-phosphate (18), (+/-)-1,3-dihydroxy-2-butanone 3-phosphate (26), and phosphonomethyl glycolate (31)).The syntheses of 18 and 26 are based on a new reaction: that is, the introduction of the phosphate group by the reaction of a diazo ketone with dibenzyl phosphate.These methods provide easy access to a number of compounds that are potential substrates for the synthetically useful enzyme aldolase (fructose-1,6-diphosphate aldolase from rabbit muscle, EC 4.1.2.13, RAMA) and perhaps for other enzymes of glycolysis.This paper also describes syntheses of 14 aldehydes for examination as substrates for aldolase.When the precursor was available, ozonolysis of vinyl groups proved to be the best route to the corresponding aldehydes.