74931-56-9

Basic information

• Product Name: Pyrrolidine, 1-(1-oxo-2-phenylpropyl)-
• CAS NO: 74931-56-9
• Molecular Formula: C13H17NO
• Molecular Weight: 203.284
• Mol File: 74931-56-9.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Pyrrolidine, 1-(1-oxo-2-phenylpropyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrrolidine, 1-(1-oxo-2-phenylpropyl)-(74931-56-9)
• EPA Substance Registry System: Pyrrolidine, 1-(1-oxo-2-phenylpropyl)-(74931-56-9)

Safety Data

• Hazardous Substances Data: 74931-56-9(Hazardous Substances Data)

Upstream product

• 67174-26-9 diphenyl N-<2-phenyl-1-(1-pyrrolidinyl)propylidene>phosphoramidate 
• 123-75-1 pyrrolidine 
• 25145-43-1 2-phenylpropionyl chloride 
• 492-37-5 hydratropic acid 
• 148932-08-5 α-Pyrrolidino-β-methyl styrene 
• 512-56-1 trimethyl phosphite 
• 3389-53-5 phenylacetylpyrrolidine 
• 100-42-5 styrene 
• 201230-82-2 carbon monoxide 
• 492-38-6 2-phenylacrylic acid 
• 26386-88-9 diphenyl phosphoryl azide 

Downstream Products

• 50888-81-8 α-Methyl-β-pyrrolidino styrene 
• 2042-85-5 1,2-diphenylpropan-1-one 
• 107644-82-6 (S)-2-Hydroxy-2-phenyl-1-pyrrolidin-1-yl-propan-1-one 
• 107644-83-7 (R)-2-Hydroxy-2-phenyl-1-pyrrolidin-1-yl-propan-1-one 

Relevant articles and documents

Preparation of alkylated compounds using the trialkylphosphate

[Problem] trialkylphosphate strong base used reaction agent, a carboxylic acid, a ketone, an aldehyde, amine, amide, thiol, ester or Grignard reagent to a variety of substrates, and/or high efficiency to generate a highly stereoselective alkylation reaction, the alkylated compounds capable of producing new means. [Solution] was used as the alkylating agent in the alkylation of compound trialkylphosphate, strongly basic reaction production use. [Drawing] no

Erratum: Photoenzymatic Reductions Enabled by Direct Excitation of Flavin-Dependent 'Ene'-Reductases (J. Am. Chem. Soc. (2021) 143:4 (1735-1739) DOI: 10.1021/jacs.0c11494)

Support by the Department of Energy was inadvertently left out of the Acknowledgments and a coauthor's name was misspelled in the Supporting Information. The scientific part of the manuscript remains unchanged. The complete correct Acknowledgment paragraph is as follows.

Palladium-catalyzed highly regioselective hydroaminocarbonylation of aromatic alkenes to branched amides

Pd(t-Bu3P)2 has been successfully identified as an efficient catalyst for the hydroaminocarbonylation of aromatic alkenes to branched amides under relatively mild reaction conditions. With hydroxylamine hydrochloride as an additive,