217447-41-1

Basic information

• Product Name: methyl 5,5-dimethoxy-3-oxopentanoate
• Synonyms: methyl 5,5-dimethoxy-3-oxopentanoate
• CAS NO: 217447-41-1
• Molecular Weight: 0
• Mol File: 217447-41-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: methyl 5,5-dimethoxy-3-oxopentanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 5,5-dimethoxy-3-oxopentanoate(217447-41-1)
• EPA Substance Registry System: methyl 5,5-dimethoxy-3-oxopentanoate(217447-41-1)

Safety Data

• Hazardous Substances Data: 217447-41-1(Hazardous Substances Data)

Upstream product

• 38330-80-2 monomethyl monopotassium malonate 
• 6191-98-6 3,3-dimethoxypropionic acid 
• 7424-91-1 methyl 3,3-dimethoxypropionate 

Downstream Products

• 1412806-89-3 C₁₈H₂₁NO₅ 
• 1412806-82-6 C₁₈H₂₁NO₅ 
• 1359869-26-3 C₁₈H₂₃NO₅ 
• 1412806-96-2 C₁₈H₂₃NO₅ 
• 496841-09-9 (2R,3R)-3-Hydroxy-pyrrolidine-2-carboxylic acid methyl ester; compound with trifluoro-acetic acid 
• 217447-50-2 (3R,4R)-4-Hydroxy-2,3,4,5-tetrahydro-pyridazine-3-carboxylic acid methyl ester 

Relevant articles and documents

TETRAHYDROPYRAZOLO-PYRAZINYL-DIHYDROIMIDAZOLONE OR TETRAHYDROPYRAZOLO-PYRIDINYL-DIHYDROIMIDAZOLONE COMPOUNDS AND METHODS OF USING SAME

The application relates to a compound of Formula (I) : or a pharmaceutically acceptable salt, hydrate, solvate, prodrug, stereoisomer, or tautomer thereof, which modulates the activity of GLP-1 receptor, a pharmaceutical composition comprising a compound of Formula (I), and a method of treating or preventing a disease in which GLP-1 receptor plays a role.

HEPATITIS C VIRUS INHIBITORS

The present disclosure relates to compounds, compositions and methods for the treatment of Hepatitis C virus (HCV) infection. Also disclosed are pharmaceutical compositions containing such compounds and methods for using these compounds in the treatment of HCV infection.

Bronsted acid mediated cyclization of enaminones. Rapid and efficient access to the tetracyclic framework of the strychnos alkaloids

The development of an efficient diastereoselective method that permits rapid construction of the tetracyclic core 17 of the Strychnos-Aspidosperma alkaloids is described. Enaminone 16, synthesized in high yield, has been cyclized under the influence of a Bronsted acid to provide the core tetracyclic framework 17 of the Strychnos alkaloids in optically active form or alternatively to the β-ketoester tetrahydro-β-carboline (THBC) unit 18, by varying the equivalents of acid and the molar concentration. Attempts to utilize 18 to form the C(7)-C(16) bond of the akuammiline related alkaloids represented by strictamine (22), using metal-carbenoid chemistry, are also described.