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Home  > Chemistry  > Asymmetric Synthesis  > Chiral Building Blocks  > (1R,3S)-3-Aminocyclopentanol

AE08941

1110772-05-8 | (1R,3S)-3-Aminocyclopentanol

Packsize Purity Availability Price Discounted Price    Quantity
10mg ≥95% in stock $42.00 $29.00 -   +
50mg ≥95% in stock $141.00 $99.00 -   +
100mg 98% in stock $147.00 $103.00 -   +
250mg 98% in stock $256.00 $179.00 -   +
1g 98% in stock $487.00 $341.00 -   +
5g 98% in stock $1,053.00 $737.00 -   +
10g 98% in stock $1,746.00 $1,222.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE08941
Chemical Name: (1R,3S)-3-Aminocyclopentanol
CAS Number: 1110772-05-8
Molecular Formula: C5H11NO
Molecular Weight: 101.1469
MDL Number: MFCD11052498
SMILES: C1CC(CC1N)O

 

Computed Properties
Complexity: 65.1  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 7  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
XLogP3: -0.4  

 

 

Upstream Synthesis Route
  • To emphasize the utility of (1R,3S)-3-Aminocyclopentanol in chemical synthesis, it is imperative to recognize its significant role as a versatile building block. This compound serves as a valuable chiral intermediate in the preparation of various complex molecules due to its unique stereochemistry and functional groups. In chemical synthesis, (1R,3S)-3-Aminocyclopentanol can be employed as a key starting material for the construction of biologically active compounds, pharmaceuticals, and agrochemicals. Its ability to participate in diverse synthetic transformations, such as condensation reactions, nucleophilic additions, and asymmetric catalysis, makes it a crucial component in the creation of intricate chemical structures.Furthermore, the presence of the amino group in (1R,3S)-3-Aminocyclopentanol offers opportunities for further derivatization, enabling the introduction of additional functionalities or enhancing the selectivity of reactions. This compound's unique molecular architecture and stereochemistry make it a valuable asset in advanced organic synthesis strategies aimed at accessing complex molecular scaffolds efficiently and selectively.
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