614754-01-7

Basic information

• Product Name: 2-Piperidinone,3-(acetyloxy)-(9CI)
• Synonyms: 2-Piperidinone,3-(acetyloxy)-(9CI)
• CAS NO: 614754-01-7
• Molecular Formula: C7H11NO3
• Molecular Weight: 157.168
• Product Categories: METHOXY
• Mol File: 614754-01-7.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Piperidinone,3-(acetyloxy)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Piperidinone,3-(acetyloxy)-(9CI)(614754-01-7)
• EPA Substance Registry System: 2-Piperidinone,3-(acetyloxy)-(9CI)(614754-01-7)

Safety Data

• Hazardous Substances Data: 614754-01-7(Hazardous Substances Data)

Upstream product

• 34433-86-8 3-bromo-2-piperidinone 
• 127-08-2 potassium acetate 
• 89180-84-7 2,5-Dibromopentanoic Acid Bromide 
• 614754-00-6 2,5-dibromovaleramide 
• 64-19-7 acetic acid 
• 463362-69-8 3-diazo-piperidin-2-one 
• 26228-95-5 3,3-dibromopiperidin-2-one 
• 675-20-7 piperidin-2-one 

Downstream Products

• 19365-08-3 3-hydroxypiperidin-2-one 

Relevant articles and documents

PYRIDINE DERIVATIVE AS ASK1 INHIBITOR AND PREPARATION METHOD AND USE THEREOF

Disclosed in the present invention are a compound as shown in formula (II), a tautomer or a pharmaceutically acceptable salt thereof, and also disclosed is the use thereof in preparing a drug for treating an ASK1-associated disease.

Photochemical rearrangement of N -chlorolactams: A route to N -heterocycles through concerted ring contraction

We report a novel ring contraction allowing the direct conversion of N-chlorolactams to their corresponding ring-contraction N-heterocycles upon photolysis. Results show that the rearrangement occurs with a variety of N-chlorolactams and that the greater the substitution at the migrating carbon, the greater the yield of product. Importantly, stereochemistry at the migrating carbon is conserved in the product. Rearranged products were isolated as their methyl carbamates in yields varying from 17% to 58%, with the major side product being the recyclable parent lactam.

Chemoenzymatic enantioselective synthesis of 3-hydroxy-2-pyrrolidinones and 3-hydroxy-2-piperidinones

The enantioselective synthesis of 3-hydroxypyrrolidin-2-ones and 3-hydroxy piperidin-2-ones has been carried out in high enantiomeric excess employing immobilized lipase from Pseudomonas cepacia.