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AE08360

1187931-23-2 | (R)-2-Aminomethyl-1-n-cbz-pyrrolidine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $33.00 $23.00 -   +
1g 95% in stock $43.00 $30.00 -   +
5g 95% in stock $123.00 $86.00 -   +
10g 95% in stock $196.00 $138.00 -   +
25g 95% in stock $466.00 $327.00 -   +
100g 95% in stock $1,504.00 $1,053.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE08360
Chemical Name: (R)-2-Aminomethyl-1-n-cbz-pyrrolidine
CAS Number: 1187931-23-2
Molecular Formula: C13H18N2O2
Molecular Weight: 234.29422000000002
MDL Number: MFCD06796560
SMILES: NC[C@H]1CCCN1C(=O)OCc1ccccc1

 

Computed Properties
Complexity: 252  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 4  
XLogP3: 1.2  

 

 

Upstream Synthesis Route
  • (R)-Benzyl 2-(aminomethyl)pyrrolidine-1-carboxylate, also known as $name$, is a versatile compound widely employed in chemical synthesis due to its unique structural characteristics and diverse reactivity. In organic synthesis, $name$ serves as a valuable chiral building block, enabling the introduction of chirality into target molecules with high enantioselectivity. This compound is particularly valuable in asymmetric synthesis, where the stereochemistry of the final product is crucial.The presence of the benzyl and pyrrolidine moieties in $name$ confers both stability and reactivity, making it an ideal substrate for a variety of synthetic transformations. The amino group offers a site for further functionalization, allowing for the rapid construction of complex molecular architectures. Additionally, the pyrrolidine ring imparts conformational rigidity, influencing the stereochemical outcome of reactions involving $name$.One notable application of (R)-Benzyl 2-(aminomethyl)pyrrolidine-1-carboxylate is in the synthesis of pharmaceutical intermediates and natural products. The chiral nature of this compound makes it a valuable tool in the pharmaceutical industry for the production of enantiopure drug molecules. By incorporating $name$ into synthetic routes, chemists can access a wide range of biologically active compounds with high purity and stereochemical control.Overall, (R)-Benzyl 2-(aminomethyl)pyrrolidine-1-carboxylate is a key component in the toolbox of synthetic chemists, enabling the efficient and stereocontrolled construction of complex molecules for various applications in chemical and pharmaceutical industries.
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