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Home  > 3-Formyl-3,4-dihydro-1h-isoquinoline-2-carboxylic acid tert-butyl ester

AD48307

104668-15-7 | 3-Formyl-3,4-dihydro-1h-isoquinoline-2-carboxylic acid tert-butyl ester

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% 2 weeks $277.00 $194.00 -   +
500mg 97% 2 weeks $408.00 $285.00 -   +
1g 97% 2 weeks $610.00 $427.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD48307
Chemical Name: 3-Formyl-3,4-dihydro-1h-isoquinoline-2-carboxylic acid tert-butyl ester
CAS Number: 104668-15-7
Molecular Formula: C15H19NO3
Molecular Weight: 261.3163
MDL Number: MFCD06738673
SMILES: O=CC1Cc2ccccc2CN1C(=O)OC(C)(C)C

 

Upstream Synthesis Route
  • tert-Butyl 3-formyl-3,4-dihydroisoquinoline-2(1H)-carboxylate is a versatile compound commonly used in chemical synthesis processes. Its application in organic chemistry involves its utilization as a key building block for the synthesis of various biologically active molecules. This compound serves as a crucial intermediate in the preparation of pharmaceuticals, agrochemicals, and materials with specialized properties.One of the prominent uses of tert-Butyl 3-formyl-3,4-dihydroisoquinoline-2(1H)-carboxylate is in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. By incorporating this compound into synthetic routes, chemists can access diverse chemical structures with potential pharmacological activities. Additionally, tert-Butyl 3-formyl-3,4-dihydroisoquinoline-2(1H)-carboxylate can participate in reactions that enable the introduction of functional groups, facilitating further derivatization and molecular modification.Moreover, this compound can serve as a valuable starting material for the construction of complex molecules through multistep synthesis. Its unique structural features contribute to the overall efficiency and selectivity of these synthetic processes. Furthermore, tert-Butyl 3-formyl-3,4-dihydroisoquinoline-2(1H)-carboxylate demonstrates good compatibility with a variety of reaction conditions, making it a versatile tool in the hands of synthetic chemists aiming to access novel compounds with diverse applications.
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