logo
Home  > Chemistry  > Asymmetric Synthesis  > Chiral Building Blocks  > (2R,4R)-1-Boc-2-hydroxymethyl-4-amino pyrrolidine-hcl

AA15165

1161931-71-0 | (2R,4R)-1-Boc-2-hydroxymethyl-4-amino pyrrolidine-hcl

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $142.00 $99.00 -   +
250mg 95% in stock $279.00 $195.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA15165
Chemical Name: (2R,4R)-1-Boc-2-hydroxymethyl-4-amino pyrrolidine-hcl
CAS Number: 1161931-71-0
Molecular Formula: C10H20N2O3
Molecular Weight: 216.2774
MDL Number: MFCD11101163
SMILES: OC[C@H]1C[C@H](CN1C(=O)OC(C)(C)C)N

 

Computed Properties
Complexity: 237  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route
  • The (2R,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride is a versatile compound commonly utilized in chemical synthesis processes. This particular molecule serves as a key building block for the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique stereochemistry and functional groups make it a valuable intermediate in the synthesis of complex organic compounds.In organic chemistry reactions, (2R,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride can act as a chiral template, facilitating the formation of new chiral centers with high stereocontrol. This property is particularly advantageous in the synthesis of biologically active molecules where precise stereochemistry is crucial for their activity and efficacy.Moreover, this compound can be employed in the preparation of peptide analogs, nucleoside derivatives, and heterocyclic scaffolds. Its Boc (tert-butoxycarbonyl) protecting group can be selectively removed under mild conditions, allowing for further functionalization of the molecule in various chemical transformations.Overall, the (2R,4R)-1-Boc-2-Hydroxymethyl-4-aminopyrrolidine hydrochloride plays a significant role in the realm of chemical synthesis, enabling the efficient construction of diverse and complex organic molecules with defined stereochemistry and biological properties.
FEATURED PRODUCTS