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Home  > 5-Bromo-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid methyl ester hcl

AV76356

1219210-17-9 | 5-Bromo-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid methyl ester hcl

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $226.00 $158.00 -   +
1g 97% in stock $403.00 $282.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AV76356
Chemical Name: 5-Bromo-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid methyl ester hcl
CAS Number: 1219210-17-9
Molecular Formula: C11H13BrClNO2
Molecular Weight: 306.5834
MDL Number: MFCD09878770
SMILES: COC(=O)C1NCc2c(C1)c(Br)ccc2.Cl

 

Computed Properties
Complexity: 247  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 1  

 

 

Upstream Synthesis Route
  • Methyl 5-bromo-1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride is a highly versatile chemical compound that is commonly employed in chemical synthesis processes. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. Its strategic molecular structure enables it to participate in diverse synthetic reactions, facilitating the formation of complex molecules with specific properties and functionalities.In chemical synthesis, the application of Methyl 5-bromo-1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride is particularly notable in the construction of heterocyclic compounds, which are prevalent in many biologically active molecules. By serving as a key intermediate, this compound contributes to the preparation of novel substances with desired pharmacological or agricultural properties. Its incorporation into synthetic routes allows for the efficient creation of structurally intricate compounds through various transformations such as cyclization, substitution, and functional group interconversions.Furthermore, Methyl 5-bromo-1,2,3,4-tetrahydroisoquinoline-3-carboxylate hydrochloride demonstrates excellent reactivity and compatibility with a wide range of synthetic methodologies, making it a valuable tool for chemists engaged in medicinal chemistry, material science, and chemical biology research. Its utility extends beyond traditional organic synthesis as it enables the synthesis of compounds with diverse applications, including drug discovery, molecular probes, and advanced materials development. By harnessing the synthetic potential of this compound, researchers can access novel molecules that hold promise for addressing various scientific and industrial challenges.
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