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AA19274

114676-69-6 | Methyl cis-1-Boc-4-hydroxy-D-prolinate

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $15.00 $10.00 -   +
1g 95% in stock $16.00 $11.00 -   +
5g 95% in stock $18.00 $12.00 -   +
10g 95% in stock $22.00 $16.00 -   +
25g 95% in stock $34.00 $24.00 -   +
250g 95% in stock $333.00 $233.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA19274
Chemical Name: Methyl cis-1-Boc-4-hydroxy-D-prolinate
CAS Number: 114676-69-6
Molecular Formula: C11H19NO5
Molecular Weight: 245.2723
MDL Number: MFCD00797548
SMILES: COC(=O)[C@H]1C[C@H](CN1C(=O)OC(C)(C)C)O

 

Computed Properties
Complexity: 310  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 4  
XLogP3: 0.6  

 

 

Upstream Synthesis Route
  • Methyl (2R,4R)-1-(tert-butyloxycarbonyl)-4-hydroxypyrrolidine-2-carboxylate is a key intermediate in chemical synthesis, specifically used in the production of pharmaceuticals and fine chemicals. This compound plays a crucial role in the construction of complex molecules due to its unique structural properties and reactivity.In chemical synthesis, Methyl (2R,4R)-1-(tert-butyloxycarbonyl)-4-hydroxypyrrolidine-2-carboxylate acts as a versatile building block for the creation of various drug candidates and bioactive compounds. Its chirality and functional groups make it an ideal starting material for the asymmetric synthesis of pharmaceutical intermediates.Furthermore, this compound serves as a valuable tool in the development of new synthetic methodologies and strategies for efficient molecule production. Its presence in the synthesis pathway can enable the formation of diverse chemical bonds and facilitate the creation of structurally intricate molecules.Overall, Methyl (2R,4R)-1-(tert-butyloxycarbonyl)-4-hydroxypyrrolidine-2-carboxylate is an indispensable component in chemical synthesis, allowing chemists to access a wide range of molecular structures with potential applications in the pharmaceutical and chemical industries.
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