124650-98-2

Basic information

• Product Name: (1S,5R,7S)-1,3,5,7-Tetramethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 6-pentafluorophenyloxycarbonyl-naphthalen-2-yl ester
• Synonyms: (1S,5R,7S)-1,3,5,7-Tetramethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 6-pentafluorophenyloxycarbonyl-naphthalen-2-yl ester
• CAS NO: 124650-98-2
• Molecular Weight: 589.516
• Mol File: 124650-98-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,5R,7S)-1,3,5,7-Tetramethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 6-pentafluorophenyloxycarbonyl-naphthalen-2-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,5R,7S)-1,3,5,7-Tetramethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 6-pentafluorophenyloxycarbonyl-naphthalen-2-yl ester(124650-98-2)
• EPA Substance Registry System: (1S,5R,7S)-1,3,5,7-Tetramethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 6-pentafluorophenyloxycarbonyl-naphthalen-2-yl ester(124650-98-2)

Safety Data

• Hazardous Substances Data: 124650-98-2(Hazardous Substances Data)

Upstream product

• 124650-94-8 (1S,5R,7S)-1,3,5,7-Tetramethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 6-methoxymethoxycarbonyl-naphthalen-2-yl ester 
• 124650-95-9 (1S,5R,7S)-1,3,5,7-Tetramethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 6-carboxy-naphthalen-2-yl ester 
• 124650-92-6 (1S,5R,7S)-1,3,5,7-Tetramethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carbonyl chloride 
• 124650-93-7 methoxymethyl 6-acetoxy-2-naphthoate 
• 124650-97-1 methoxymethyl 6-hydroxy-2-naphthoate 
• 17295-26-0 6-acetoxy-2-naphthoic acid 
• 16712-64-4 6-Hydroxy-2-naphthoic acid 
• 124650-96-0 (1S,5R,7S)-1,3,5,7-Tetramethyl-2,4-dioxo-3-aza-bicyclo[3.3.1]nonane-7-carboxylic acid 6-chlorocarbonyl-naphthalen-2-yl ester 

Relevant articles and documents

Kinetic studies and modeling of a self-replicating system

The design, synthesis, and study of a molecular template, 11a, that catalyzes its own formation from simpler components, 9 and 10d, is described. Autocatalysis is shown by the following: (1) the increase in rate of reaction of 9 and 10d in the presence of 11a; (2) the reduction in rate of reaction in the presence of 2,6-bis(acetylamino)pyridine inhibitor; and (3) the reduction in rate of reaction when a component incapable of template behavior, 10b, is substituted for 10d. Three kinetic pathways are elucidated: (1) the background bimolecular reaction (eq 6); (2) the preassociative mechanism (eq 7); and (3) the template termolecular process (eq 8). A kinetic model for the replication process is introduced, and equilibrium and rate constants are determined. Predictions for the shapes of the product growth curves are made.