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Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aliphatic Heterocycles  > Methyl (1r,5s,6r)-3-azabicyclo[3.1.0]hexane-6-carboxylate hydrochloride

AA09360

1024038-72-9 | Methyl (1r,5s,6r)-3-azabicyclo[3.1.0]hexane-6-carboxylate hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $306.00 $214.00 -   +
5g 95% in stock $1,178.00 $824.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA09360
Chemical Name: Methyl (1r,5s,6r)-3-azabicyclo[3.1.0]hexane-6-carboxylate hydrochloride
CAS Number: 1024038-72-9
Molecular Formula: C7H12ClNO2
Molecular Weight: 177.6287
MDL Number: MFCD11099878
SMILES: COC(=O)[C@@H]1[C@@H]2[C@H]1CNC2.Cl

 

Computed Properties
Complexity: 159  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 2  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • 3-Azabicyclo[3.1.0]hexane-6-carboxylic acid, methyl ester, (1α,5α,6α) is a valuable compound widely used in chemical synthesis as a versatile building block for the creation of complex molecules. Due to its unique structure and properties, this compound serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its bicyclic nature and chirality make it a valuable scaffold for designing molecules with specific biological activities.In chemical synthesis, this compound can participate in a range of reactions including esterification, hydrolysis, and substitution reactions to introduce functional groups at specific positions along the bicyclic ring system. The presence of the carboxylic acid and methyl ester functionalities allows for further derivatization, enabling the synthesis of diverse molecular structures with tailored properties.Moreover, the 1α,5α,6α configuration of this compound imparts stereochemical control in reactions, facilitating the construction of enantioenriched or diastereomerically pure products. This high level of stereochemical fidelity is crucial in the synthesis of biologically active compounds where the spatial arrangement of atoms greatly influences their interactions with biological targets.Overall, 3-Azabicyclo[3.1.0]hexane-6-carboxylic acid, methyl ester, (1α,5α,6α) is a valuable tool in the arsenal of synthetic chemists, enabling the efficient and strategic construction of complex molecules with desired structural and stereochemical features. Its versatility and utility make it a key component in the synthesis of novel compounds for various applications in the fields of medicine, agriculture, and materials science.
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