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Home  > Chemistry  > Asymmetric Synthesis  > Chiral Building Blocks  > (1R,2R)-(-)-2-Benzyloxycyclohexylamine

AB54600

216394-06-8 | (1R,2R)-(-)-2-Benzyloxycyclohexylamine

Packsize Purity Availability Price Discounted Price    Quantity
1g 97% in stock $30.00 $21.00 -   +
5g 97% in stock $91.00 $64.00 -   +
10g 97% in stock $179.00 $125.00 -   +
25g 97% in stock $364.00 $255.00 -   +
100g 97% in stock $1,094.00 $766.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB54600
Chemical Name: (1R,2R)-(-)-2-Benzyloxycyclohexylamine
CAS Number: 216394-06-8
Molecular Formula: C13H19NO
Molecular Weight: 205.2960600000001
MDL Number: MFCD01075752
SMILES: N[C@@H]1CCCC[C@H]1OCc1ccccc1

 

Computed Properties
Complexity: 177  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  
XLogP3: 2  

 

 

Upstream Synthesis Route
  • Cyclohexanamine, 2-(phenylmethoxy)-, (1R,2R)- is a versatile compound widely utilized in chemical synthesis processes. Its chirality, represented by the (1R,2R) configuration, makes it particularly valuable for the development of enantioselective reactions.In organic chemistry, Cyclohexanamine, 2-(phenylmethoxy)-, (1R,2R)- serves as a chiral building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure and reactivity enable the creation of complex molecular structures with high levels of stereochemical control. This compound is frequently employed in asymmetric transformations, including catalytic hydrogenation, metal-catalyzed reactions, and organocatalysis.Furthermore, Cyclohexanamine, 2-(phenylmethoxy)-, (1R,2R)- can act as a versatile intermediate in the preparation of chiral ligands, ligand precursors, and other valuable compounds used in advanced chemical transformations. Its role in facilitating the creation of enantiopure molecules highlights its significance in modern synthetic organic chemistry.
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