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AB56188

104612-35-3 | (S)-3-Hydroxy-1-methylpyrrolidine-2,5-dione

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $80.00 $56.00 -   +
1g 98% in stock $236.00 $165.00 -   +
5g 98% in stock $941.00 $659.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB56188
Chemical Name: (S)-3-Hydroxy-1-methylpyrrolidine-2,5-dione
CAS Number: 104612-35-3
Molecular Formula: C5H7NO3
Molecular Weight: 129.114
MDL Number: MFCD00221501
SMILES: O[C@H]1CC(=O)N(C1=O)C

 

Computed Properties
Complexity: 166  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
XLogP3: -1.4  

 

 

Upstream Synthesis Route
  • The compound (3S)-3-Hydroxy-1-methyl-2,5-pyrrolidinedione, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. With its unique structure and reactivity, $name$ serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, (3S)-3-Hydroxy-1-methyl-2,5-pyrrolidinedione is widely utilized in the formation of complex molecules through strategic bond formation and functional group transformations. Its presence in a reaction mixture can facilitate the creation of diverse molecular architectures with high stereochemical control, making it an indispensable component in the toolkit of synthetic chemists. Additionally, (3S)-3-Hydroxy-1-methyl-2,5-pyrrolidinedione enables the construction of chiral compounds, which are of utmost importance in drug discovery and development processes. Its ability to participate in asymmetric synthesis further enhances its value in generating enantiomerically pure compounds of pharmaceutical interest. By harnessing the synthetic utility of (3S)-3-Hydroxy-1-methyl-2,5-pyrrolidinedione, chemists can streamline the production of intricate molecules and contribute to advancements in the field of organic chemistry.
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