1122-35-6

Basic information

• Product Name: 2-Pyrrolidinone, 1-(1-propenyl)-
• CAS NO: 1122-35-6
• Molecular Formula: C7H11NO
• Molecular Weight: 125.17
• Mol File: 1122-35-6.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 2-Pyrrolidinone, 1-(1-propenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Pyrrolidinone, 1-(1-propenyl)-(1122-35-6)
• EPA Substance Registry System: 2-Pyrrolidinone, 1-(1-propenyl)-(1122-35-6)

Safety Data

• Hazardous Substances Data: 1122-35-6(Hazardous Substances Data)

Upstream product

• 42366-62-1 1-(2-chloro-propyl)-pyrrolidin-2-one 
• 2687-97-0 1-allyl-2-pyrrolidinone 
• 4204-66-4 1-(2-hydroxy-propyl)-pyrrolidin-2-one 
• 616-45-5 2-pyrrolidinon 
• 123-38-6 propionaldehyde 

Downstream Products

• 616-45-5 2-pyrrolidinon 

Relevant articles and documents

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One-step RhCl3-catalyzed deprotection of acyclic N-allyl amides

(Chemical Equation Presented) A convenient one-step RhCl 3-catalyzed deprotection of acyclic N-allyl amides is described. Preliminary mechanistic studies reveal that the key to the success of the one-step deprotection process is the dual function of RhCl3 in alcohol solvents. Reaction of RhCl3 with n-PrOH not only provides an active rhodium hydride species to catalyze isomerization of N-allyl amides to corresponding enamides but also generates a crucial catalytic amount of HCl to convert the enamides to deallylated amides through N,O-acetal exchange.

XtalFluor-E mediated proto-functionalization of: N -vinyl amides: Access to N -acetyl N, O -acetals

XtalFluor-E has been extensively used in a broad range of reactions in the past few years. Here we report its use with protic nucleophiles in a catalytic manner for the in situ generation of protons that lead to the proto-functionalization of activated ol

TFA-catalyzed C-N bond activation of enamides with indoles: Efficient synthesis of 3,3-bisindolylpropanoates and other bisindolylalkanes

An efficient TFA-catalyzed cleavage of C-N bonds in alkylation of indoles by tertiary enamides was described. A variety of bisindolylalkane derivatives, especially 3,3-bisindolylpropanoates, were expeditiously synthesized in good yields.