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Home  > 6-Bromo-3,4-dihydro-2h-isothiochromen-4-amine hcl

AD74243

1187830-57-4 | 6-Bromo-3,4-dihydro-2h-isothiochromen-4-amine hcl

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $297.00 $208.00 -   +
250mg 95% in stock $341.00 $239.00 -   +
1g 95% in stock $834.00 $584.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD74243
Chemical Name: 6-Bromo-3,4-dihydro-2h-isothiochromen-4-amine hcl
CAS Number: 1187830-57-4
Molecular Formula: C9H11BrClNS
Molecular Weight: 280.6123
MDL Number: MFCD09878672
SMILES: Brc1ccc2c(c1)C(N)CSC2.Cl

 

Computed Properties
Complexity: 165  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 2  
Undefined Atom Stereocenter Count: 1  

 

 

Upstream Synthesis Route
  • 6-Bromoisothiochroman-4-amine hydrochloride is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. This compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and materials. Specifically, its amine and bromine functional groups make it a valuable intermediate in the synthesis of bioactive molecules and heterocyclic scaffolds.In chemical synthesis, 6-Bromoisothiochroman-4-amine hydrochloride is often employed as a nucleophilic or electrophilic reagent in cross-coupling reactions, halogenation processes, and substitution reactions. Additionally, its presence can facilitate the introduction of diverse functional groups into organic molecules, allowing for the creation of complex molecular structures with precise stereochemistry.Furthermore, the compatibility of 6-Bromoisothiochroman-4-amine hydrochloride with a variety of reaction conditions makes it a versatile tool for organic chemists seeking to design and construct novel compounds with tailored physicochemical properties. Its selective reactivity and ease of manipulation contribute to its widespread utility in the field of chemical synthesis.
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