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Home  > N-Boc-trans-4-fluoro-l-proline methyl ester

AB04978

203866-18-6 | N-Boc-trans-4-fluoro-l-proline methyl ester

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $13.00 $9.00 -   +
5g 95% in stock $33.00 $23.00 -   +
10g 95% in stock $60.00 $42.00 -   +
25g 95% in stock $127.00 $89.00 -   +
50g 95% in stock $239.00 $167.00 -   +
100g 95% in stock $462.00 $324.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB04978
Chemical Name: N-Boc-trans-4-fluoro-l-proline methyl ester
CAS Number: 203866-18-6
Molecular Formula: C11H18FNO4
Molecular Weight: 247.2633
MDL Number: MFCD07367993
SMILES: COC(=O)[C@@H]1C[C@H](CN1C(=O)OC(C)(C)C)F

 

Computed Properties
Complexity: 313  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 5  
Rotatable Bond Count: 4  
XLogP3: 1.6  

 

 

Upstream Synthesis Route
  • (2S,4R)-1-tert-Butyl 2-methyl 4-fluoropyrrolidine-1,2-dicarboxylate is a versatile compound widely used in chemical synthesis. Its unique stereochemistry and functional groups make it an ideal building block for the creation of complex molecules in organic chemistry. This compound is particularly valuable in the development of pharmaceuticals, agrochemicals, and advanced materials due to its structural characteristics that can impart specific properties and activities to the final products. In chemical synthesis, (2S,4R)-1-tert-Butyl 2-methyl 4-fluoropyrrolidine-1,2-dicarboxylate serves as a key intermediate for the construction of diverse molecular architectures through strategic bond formations and transformations. Its presence in a synthesis pathway can enable the introduction of the tert-butyl, methyl, and fluoropyrrolidine functional groups with precise control over stereochemistry, leading to the creation of novel and potentially bioactive compounds.
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