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AA01509

1002355-96-5 | tert-Butyl 3-(2-ethoxy-2-oxoethylidene)azetidine-1-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $17.00 $12.00 -   +
5g 95% in stock $46.00 $33.00 -   +
10g 95% in stock $90.00 $63.00 -   +
25g 95% in stock $182.00 $127.00 -   +
250g 95% in stock $1,654.00 $1,158.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA01509
Chemical Name: tert-Butyl 3-(2-ethoxy-2-oxoethylidene)azetidine-1-carboxylate
CAS Number: 1002355-96-5
Molecular Formula: C12H19NO4
Molecular Weight: 241.2836
MDL Number: MFCD16140210
SMILES: CCOC(=O)C=C1CN(C1)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 333  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 5  
XLogP3: 0.8  

 

 

Upstream Synthesis Route
  • The tert-Butyl 3-(2-ethoxy-2-oxoethylidene)azetidine-1-carboxylate compound serves as a valuable reagent in chemical synthesis due to its unique structure and versatile reactivity. With its azetidine ring and ester functionality, this compound can participate in a wide range of organic reactions, making it a useful building block for the synthesis of various compounds. In particular, tert-Butyl 3-(2-ethoxy-2-oxoethylidene)azetidine-1-carboxylate can be employed in the synthesis of heterocyclic compounds, pharmaceutical intermediates, and agrochemicals. Its ability to undergo ring-opening reactions, ester hydrolysis, and cycloaddition reactions makes it a versatile tool for organic chemists looking to create complex molecules with specific functionalities. Additionally, the tert-Butyl group provides steric hindrance, which can influence the regioselectivity and stereochemistry of the reactions it undergoes. Overall, tert-Butyl 3-(2-ethoxy-2-oxoethylidene)azetidine-1-carboxylate is a valuable compound in organic synthesis, enabling the efficient construction of diverse chemical structures for various applications in the field of chemistry.
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