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AB55683

106973-36-8 | (R)-4-Benzyl-5-oxo-3-morpholinecarboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $23.00 $16.00 -   +
2g 95% in stock $42.00 $29.00 -   +
5g 95% in stock $69.00 $48.00 -   +
10g 95% in stock $135.00 $94.00 -   +
15g 95% in stock $199.00 $139.00 -   +
25g 95% in stock $296.00 $207.00 -   +
50g 95% in stock $587.00 $411.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB55683
Chemical Name: (R)-4-Benzyl-5-oxo-3-morpholinecarboxylic acid
CAS Number: 106973-36-8
Molecular Formula: C12H13NO4
Molecular Weight: 235.2359
MDL Number: MFCD12031258
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
  • (R)-4-Benzyl-5-oxomorpholine-3-carboxylic acid, also known as $name$, is a versatile compound widely utilized in chemical synthesis. Its unique structure and functional groups make it a valuable building block for the creation of various pharmaceuticals, agrochemicals, and other organic compounds.In chemical synthesis, (R)-4-Benzyl-5-oxomorpholine-3-carboxylic acid serves as a crucial intermediate in the production of complex molecules. Its carboxylic acid group allows for facile derivatization, enabling the introduction of different functional groups to tailor the properties of the final product. The benzyl moiety provides stability and can participate in diverse reactions, expanding the synthetic possibilities.Moreover, the morpholine ring in the structure of (R)-4-Benzyl-5-oxomorpholine-3-carboxylic acid imparts unique properties, such as steric hindrance and potential for hydrogen bonding interactions. These characteristics are instrumental in controlling the stereochemistry and reactivity of reactions involving this compound, leading to the formation of chiral molecules with high selectivity.Overall, (R)-4-Benzyl-5-oxomorpholine-3-carboxylic acid is a valuable tool in chemical synthesis, offering versatility, reactivity, and control in the construction of intricate organic molecules. Its diverse applications make it a key component in the development of novel compounds with potential implications in pharmaceuticals, materials science, and other fields.
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