(S)-2,3,6,7-Tetrahydro-1H-Pyrazino[2,1-A]Isoquinolin-4(11Bh)-One (2S,3S)-2,3-Bis(Benzoyloxy)Succinate

98%

Reagent Code: #237227
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CAS Number 1622136-46-2

science Other reagents with same CAS 1622136-46-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 560.55 g/mol
Formula C₃₀H₂₈N₂O₉
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in pharmaceutical research as a chiral intermediate for the synthesis of bioactive compounds, particularly in the development of central nervous system agents. Its stereochemistry makes it valuable in asymmetric synthesis, where it helps control the formation of specific enantiomers in complex drug molecules. The compound’s structure supports its role in facilitating selective reactions, improving yield and purity in the production of active pharmaceutical ingredients. It is also employed in studies exploring novel isoquinoline-based therapeutics with potential applications in neurology and oncology.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,720.00
(S)-2,3,6,7-Tetrahydro-1H-Pyrazino[2,1-A]Isoquinolin-4(11Bh)-One (2S,3S)-2,3-Bis(Benzoyloxy)Succinate
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Used in pharmaceutical research as a chiral intermediate for the synthesis of bioactive compounds, particularly in the development of central nervous system agents. Its stereochemistry makes it valuable in asymmetric synthesis, where it helps control the formation of specific enantiomers in complex drug molecules. The compound’s structure supports its role in facilitating selective reactions, improving yield and purity in the production of active pharmaceutical ingredients. It is also employed in studies

Used in pharmaceutical research as a chiral intermediate for the synthesis of bioactive compounds, particularly in the development of central nervous system agents. Its stereochemistry makes it valuable in asymmetric synthesis, where it helps control the formation of specific enantiomers in complex drug molecules. The compound’s structure supports its role in facilitating selective reactions, improving yield and purity in the production of active pharmaceutical ingredients. It is also employed in studies exploring novel isoquinoline-based therapeutics with potential applications in neurology and oncology.

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