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Home  > Chemistry  > Heterocyclic Building Blocks  > Piperidines  > tert-Butyl-(3R,4R)-3-fluoro-4-hydroxy-piperidine-1-carboxylate

AA18247

1174020-43-9 | tert-Butyl-(3R,4R)-3-fluoro-4-hydroxy-piperidine-1-carboxylate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $49.00 $35.00 -   +
250mg 97% in stock $76.00 $54.00 -   +
1g 97% in stock $251.00 $176.00 -   +
5g 97% in stock $713.00 $499.00 -   +
10g 97% in stock $1,179.00 $825.00 -   +
25g 97% in stock $2,112.00 $1,479.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA18247
Chemical Name: tert-Butyl-(3R,4R)-3-fluoro-4-hydroxy-piperidine-1-carboxylate
CAS Number: 1174020-43-9
Molecular Formula: C10H18FNO3
Molecular Weight: 219.2532
MDL Number: MFCD22123259
SMILES: O[C@@H]1CCN(C[C@H]1F)C(=O)OC(C)(C)C

 

Computed Properties
Complexity: 239  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 1  

 

 

Upstream Synthesis Route
  • This specific compound, tert-Butyl (3R,4R)-3-fluoro-4-hydroxypiperidine-1-carboxylate, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure consisting of a piperidine ring with a fluoro and hydroxy substitution provides diverse functionality for creating complex molecular frameworks. In organic synthesis, this compound can serve as a key intermediate for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its suitability for asymmetric synthesis makes it particularly valuable for the creation of chiral compounds with high optical purity. Additionally, the tert-butyl protection group enhances the compound's stability and reactivity, allowing for selective transformations during chemical reactions. This compound's utility extends across a wide range of synthetic pathways, exemplifying its significance in modern chemical synthesis strategies.
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