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Home  > (S)-tert-Butyl 4-(((tert-butylsulfinyl)imino)methyl)piperidine-1-carboxylate

AX52880

1097880-26-6 | (S)-tert-Butyl 4-(((tert-butylsulfinyl)imino)methyl)piperidine-1-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $186.00 $131.00 -   +
250mg 95% in stock $310.00 $217.00 -   +
500mg 95% in stock $434.00 $304.00 -   +
1g 95% in stock $620.00 $434.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AX52880
Chemical Name: (S)-tert-Butyl 4-(((tert-butylsulfinyl)imino)methyl)piperidine-1-carboxylate
CAS Number: 1097880-26-6
Molecular Formula: C15H28N2O3S
Molecular Weight: 316.4594
MDL Number: MFCD18781720
SMILES: O=C(N1CCC(CC1)/C=N/[S@@](=O)C(C)(C)C)OC(C)(C)C

 

Computed Properties
Complexity: 414  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 21  
Hydrogen Bond Acceptor Count: 5  
Rotatable Bond Count: 5  
Undefined Bond Stereocenter Count: 1  
XLogP3: 1.7  

 

 

Upstream Synthesis Route
  • The compound (S)-Tert-Butyl 4-(((Tert-Butylsulfinyl)Imino)Methyl)Piperidine-1-Carboxylate plays a crucial role in chemical synthesis as a versatile building block with numerous applications. Its unique structure allows for selective functional group manipulations and stereochemical control, making it a valuable tool in the synthesis of complex organic molecules. Specifically, this compound is commonly utilized in the preparation of chiral piperidine derivatives and pharmaceutical intermediates. Its ability to serve as a chiral auxiliary or ligand in asymmetric catalysis reactions further enhances its utility in the creation of enantioenriched compounds. Additionally, (S)-Tert-Butyl 4-(((Tert-Butylsulfinyl)Imino)Methyl)Piperidine-1-Carboxylate can facilitate the formation of biologically active molecules through strategic transformations, making it an essential component in the toolbox of synthetic chemists.
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