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Home  > Chemistry  > Heterocyclic Building Blocks  > Morpholines  > (S)-4-Benzyl-5-oxomorpholine-3-carboxylic acid

AB56126

106973-37-9 | (S)-4-Benzyl-5-oxomorpholine-3-carboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $22.00 $16.00 -   +
1g 97% in stock $48.00 $34.00 -   +
5g 97% in stock $137.00 $96.00 -   +
10g >97% in stock $258.00 $180.00 -   +
25g >97% in stock $558.00 $390.00 -   +
100g 98% in stock $1,653.00 $1,157.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AB56126
Chemical Name: (S)-4-Benzyl-5-oxomorpholine-3-carboxylic acid
CAS Number: 106973-37-9
Molecular Formula: C12H13NO4
Molecular Weight: 235.2359
MDL Number: MFCD09835535
SMILES: OC(=O)[C@@H]1COCC(=O)N1Cc1ccccc1

 

Computed Properties
Complexity: 299  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 0.5  

 

 

Upstream Synthesis Route
  • The (S)-4-Benzyl-5-oxomorpholine-3-carboxylic acid is a valuable compound commonly utilized in chemical synthesis as a chiral building block. Due to its unique structure and chirality, this compound serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials. When incorporated into synthetic pathways, (S)-4-Benzyl-5-oxomorpholine-3-carboxylic acid enables the controlled formation of new carbon-carbon and carbon-nitrogen bonds, facilitating the creation of complex molecular structures with high stereochemical purity. Its distinct reactivity and stereochemical characteristics make it a versatile tool for the production of advanced organic molecules with specific biological or catalytic properties. By harnessing the synthetic potential of this compound, chemists can access diverse chemical space and develop innovative molecules with promising applications in drug discovery, material science, and chemical biology.
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