It also serves as a versatile scaffold in organic synthesis for developing new drugs and materials, including anticancer agents. (1S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline (THPIQ) is used mainly as a crucial chiral building block in pharmaceutical synthesis, notably for making Solifenacin (for overactive bladder), and as a lead compound in neuroscience research, studied for its potential role in Parkinson’s disease and other neurological conditions due to its interaction with dopamine pathways and neurotoxin-like properties.
(1S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline
| API Name | Solifenacin succinate |
|---|---|
| CAS No | 118864-75-8 |
| Molecular Formula | C15H15N |
| Molecular Weight | 209.29 g/mol |
| Synonyms | (1S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline |
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Frequently Asked Questions
It also serves as a versatile scaffold in organic synthesis for developing new drugs and materials, including anticancer agents. (1S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline (THPIQ) is used mainly as a crucial chiral building block in pharmaceutical synthesis, notably for making Solifenacin (for overactive bladder), and as a lead compound in neuroscience research, studied for its potential role in Parkinson's disease and other neurological conditions due to its interaction with dopamine pathways and neurotoxin-like properties.
The CAS number of (1S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline is 118864-75-8.
The molecular formula of (1S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline is C15H15N.
The listed molecular weight of (1S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline is 209.29 g/mol.
(1S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline is listed as being used in connection with the following API: Solifenacin succinate.
The listed synonym or IUPAC name for (1S)-1,2,3,4-Tetrahydro-1-phenylisoquinoline is (1S)-1-phenyl-1,2,3,4-tetrahydroisoquinoline.