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AB56116

106825-79-0 | (S)-Morpholine-3-carboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg >95% in stock $29.00 $20.00 -   +
250mg >95% in stock $55.00 $38.00 -   +
1g >95% in stock $72.00 $50.00 -   +
5g >95% in stock $169.00 $118.00 -   +
10g >95% in stock $276.00 $193.00 -   +
25g >95% in stock $565.00 $395.00 -   +
100g >95% in stock $1,715.00 $1,200.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB56116
Chemical Name: (S)-Morpholine-3-carboxylic acid
CAS Number: 106825-79-0
Molecular Formula: C5H9NO3
Molecular Weight: 131.1299
MDL Number: MFCD03426307
SMILES: OC(=O)[C@@H]1COCCN1

 

Computed Properties
Complexity: 115  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 1  
XLogP3: -3.2  

 

 

Upstream Synthesis Route
  • (S)-3-Morpholinecarboxylic Acid, also known as L-3-amino morpholine-4-carboxylic acid, is a versatile compound widely used in chemical synthesis. This chiral building block is prized for its ability to introduce chirality into various organic molecules and is particularly valuable in the pharmaceutical industry for the synthesis of chiral drugs and pharmaceutical intermediates.One of the key applications of (S)-3-Morpholinecarboxylic Acid is in the preparation of enantiomerically pure compounds. By utilizing this compound as a starting material, chemists can selectively access one enantiomer over the other, leading to the development of new pharmaceuticals with enhanced biological activity and reduced side effects. Its unique structural attributes make it an essential tool in asymmetric synthesis, enabling the efficient construction of complex molecular structures with high stereochemical control.Additionally, (S)-3-Morpholinecarboxylic Acid plays a crucial role in the synthesis of chiral ligands for asymmetric catalysis. These ligands are used in various transition metal-catalyzed reactions to facilitate the formation of enantioenriched products. By incorporating (S)-3-Morpholinecarboxylic Acid-derived ligands into catalytic systems, chemists can achieve high levels of enantioselectivity, paving the way for the synthesis of important chiral molecules in a sustainable and cost-effective manner.In summary, the application of (S)-3-Morpholinecarboxylic Acid in chemical synthesis is instrumental in the creation of enantiomerically pure compounds, chiral pharmaceuticals, and asymmetric catalytic systems. Its versatile nature and impact on stereochemistry make it a valuable asset in the toolkit of synthetic chemists striving to develop novel drugs, agrochemicals, and functional materials.
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