646055-93-8

Basic information

• Product Name: ethyl 2-aMino-2-(tetrahydro-2H-pyran-4-yl)acetate
• Synonyms: ethyl 2-aMino-2-(tetrahydro-2H-pyran-4-yl)acetate;2H-Pyran-4-acetic acid, a-aMinotetrahydro-, ethyl ester;ethyl 2-amino-2-(oxan-4-yl)acetate
• CAS NO: 646055-93-8
• Molecular Formula: C₉H₁₇NO₃
• Molecular Weight: 187.23618
• Mol File: 646055-93-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 262.1±10.0 °C(Predicted)
• Appearance: /
• Density: 1.080±0.06 g/cm3(Predicted)
• PKA: 7.40±0.50(Predicted)
• CAS DataBase Reference: ethyl 2-aMino-2-(tetrahydro-2H-pyran-4-yl)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-aMino-2-(tetrahydro-2H-pyran-4-yl)acetate(646055-93-8)
• EPA Substance Registry System: ethyl 2-aMino-2-(tetrahydro-2H-pyran-4-yl)acetate(646055-93-8)

Safety Data

• Hazardous Substances Data: 646055-93-8(Hazardous Substances Data)

Usage

Description

Ethyl 2-amino-2-(tetrahydro-2H-pyran-4-yl)acetate is a chemical compound with the molecular formula C10H17NO3. It is a derivative of ethyl acetate and contains an amino group and a tetrahydro-2H-pyran-4-yl group. ethyl 2-aMino-2-(tetrahydro-2H-pyran-4-yl)acetate can be used in organic synthesis and pharmaceutical research as a building block for creating more complex molecules. It may also have potential pharmaceutical applications due to its structure and properties. However, further research and testing would be needed to fully understand its potential uses and effects.

Uses

Used in Organic Synthesis:
Ethyl 2-amino-2-(tetrahydro-2H-pyran-4-yl)acetate is used as a building block in organic synthesis for creating more complex molecules. Its unique structure allows for various chemical reactions and modifications, making it a valuable component in the synthesis of a wide range of organic compounds.
Used in Pharmaceutical Research:
Ethyl 2-amino-2-(tetrahydro-2H-pyran-4-yl)acetate is used as a building block in pharmaceutical research for the development of new drugs. Its structure and properties may contribute to the creation of novel therapeutic agents with potential applications in various medical fields. Further research and testing are required to explore its full potential in the pharmaceutical industry.

Upstream product

• 921755-40-0 ethyl 3,6-dihydro-2H-pyran-4-yl-nitroacetate 
• 29943-42-8 Tetrahydro-4H-pyran-4-one 
• 626-35-7 nitroacetic acid ethyl ester 
• 921755-39-7 (benzhydrylidene-amino)-(tetrahydro-pyran-4-yl)-acetic acid ethyl ester 
• 25637-18-7 4-iodotetrahydropyran 

Downstream Products

• 1257388-54-7 6-(3,5-difluorophenyl)-3-(tetrahydro-2H-pyran-4-yl)piperazin-2-one 
• 1257388-50-3 ethyl (rac)-benzylamino(tetrahydropyran-4-yl)acetate 
• 792905-68-1 1-azabicyclo[2.2.1]heptane-7-carboxylic acid 

Relevant articles and documents

Synthesis of bicyclic tertiary α-amino acids

Novel bicyclic α-amino acids, exo and endo-1-azabicyclo-[2.2.1] heptane-2-carboxylic acid, 1-azabicyclo[2.2.1]heptane-7-carboxylic acid, and 1-azabicyclo[3.2.2]nonane-2-carboxylic acid have been readily synthesized for the generation of neuronal nicotinic receptor ligands. Alkylation of glycine-derived Schiff bases or nitroacetates with cyclic ether electrophiles, followed by acid-induced ring opening and cyclization in NH4OH, allowed for the preparation of substantial quantities of the three tertiary bicyclic α-amino acids.

N-ARYL DIAZASPIRACYCLIC COMPOUNDS AND METHODS OF PREPARATION AND USE THEREOF

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