1-​[(4R)​-​4,​5-​Dihydro-​4-​isopropyl​-​2-​oxazolyl]​isoquinoline

≥98%,99%e.e.

Reagent Code: #70594
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CAS Number 280755-83-1

science Other reagents with same CAS 280755-83-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.3 g/mol
Formula C₁₅H₁₆N₂O
thermostat Physical Properties
Boiling Point 407.1±18.0 °C
inventory_2 Storage & Handling
Density 1.18±0.1 g/mL
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate or building block for the synthesis of more complex molecules. Its structure, featuring a 4,5-dihydro-4-isopropyl-2-oxazolyl group attached to the 1-position of an isoquinoline moiety, makes it valuable for developing pharmaceuticals, particularly those targeting neurological disorders or acting as enzyme inhibitors. Researchers often explore its potential in designing drugs that interact with specific biological pathways, leveraging its unique chemical framework to enhance binding affinity and selectivity. Additionally, it may be employed in asymmetric synthesis due to its chiral center at the 4-position, contributing to the production of enantiomerically pure compounds. Its applications are largely experimental, focusing on drug discovery and development processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,097.00
inventory 250mg
10-20 days ฿5,004.00

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1-​[(4R)​-​4,​5-​Dihydro-​4-​isopropyl​-​2-​oxazolyl]​isoquinoline
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate or building block for the synthesis of more complex molecules. Its structure, featuring a 4,5-dihydro-4-isopropyl-2-oxazolyl group attached to the 1-position of an isoquinoline moiety, makes it valuable for developing pharmaceuticals, particularly those targeting neurological disorders or acting as enzyme inhibitors. Researchers often explore its potential in designing drugs that interact with specific biologica

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate or building block for the synthesis of more complex molecules. Its structure, featuring a 4,5-dihydro-4-isopropyl-2-oxazolyl group attached to the 1-position of an isoquinoline moiety, makes it valuable for developing pharmaceuticals, particularly those targeting neurological disorders or acting as enzyme inhibitors. Researchers often explore its potential in designing drugs that interact with specific biological pathways, leveraging its unique chemical framework to enhance binding affinity and selectivity. Additionally, it may be employed in asymmetric synthesis due to its chiral center at the 4-position, contributing to the production of enantiomerically pure compounds. Its applications are largely experimental, focusing on drug discovery and development processes.

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