logo
Home  > (S)-7-Bromo-1,2,3,4-tetrahydro-naphthalen-1-ylamine hydrochloride

AH21048

676133-24-7 | (S)-7-Bromo-1,2,3,4-tetrahydro-naphthalen-1-ylamine hydrochloride

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $30.00 $21.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AH21048
Chemical Name: (S)-7-Bromo-1,2,3,4-tetrahydro-naphthalen-1-ylamine hydrochloride
CAS Number: 676133-24-7
Molecular Formula: C10H13BrClN
Molecular Weight: 262.5739
MDL Number: MFCD22393203
SMILES: Brc1ccc2c(c1)[C@@H](N)CCC2.Cl

 

Computed Properties
Complexity: 160  
Covalently-Bonded Unit Count: 2  
Defined Atom Stereocenter Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 2  

 

 

Upstream Synthesis Route
  • The (S)-7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride serves as a valuable reagent in chemical synthesis, particularly in the synthesis of complex organic molecules. Its unique structural features make it an important building block for the development of various pharmaceuticals, agrochemicals, and other fine chemicals. By leveraging its stereochemistry and reactivity, chemists can efficiently introduce the tetrahydronaphthalene motif into target molecules, allowing for the construction of diverse chemical structures with specific biological or pharmaceutical properties.In the realm of chemical synthesis, the (S)-7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride can be employed in asymmetric transformations to access enantiomerically enriched compounds. Its bromine moiety can serve as a versatile handle for further functionalization reactions, enabling the introduction of different chemical groups at specific positions within a molecule. Additionally, the amine group in the structure can participate in various types of transformations, such as reductive aminations, reductive couplings, and reductive alkylations, expanding the synthetic possibilities of this compound.Moreover, the hydrochloride salt form of (S)-7-Bromo-1,2,3,4-tetrahydronaphthalen-1-amine offers advantages in terms of solubility and handling compared to the free amine form, making it more convenient for use in synthetic processes. Overall, the application of this compound in chemical synthesis underscores its significance as a versatile building block for the creation of diverse and complex organic molecules with tailored properties and functionalities.
FEATURED PRODUCTS