tert-Butyl 6-hydroxy-3,4-dihydroisoquinoline-2(1H)-carboxylate

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Reagent Code: #121430
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CAS Number 158984-83-9

science Other reagents with same CAS 158984-83-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.31 g/mol
Formula C₁₄H₁₉NO₃
badge Registry Numbers
MDL Number MFCD08275034
thermostat Physical Properties
Boiling Point 391.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. It is particularly valuable in the development of pharmaceuticals, as its structure can be modified to create compounds with potential therapeutic effects. Researchers often employ it in the synthesis of alkaloids and other nitrogen-containing heterocycles, which are common in many drugs. Additionally, its protective group properties make it useful in multi-step synthetic processes, ensuring specific functional groups remain unaffected during reactions. Its application extends to the study of biochemical pathways and the development of new medicinal agents targeting various diseases.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,944.00
inventory 10g
10-20 days ฿19,746.00
inventory 1g
10-20 days ฿3,879.00
inventory 5g
10-20 days ฿11,700.00

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tert-Butyl 6-hydroxy-3,4-dihydroisoquinoline-2(1H)-carboxylate
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This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. It is particularly valuable in the development of pharmaceuticals, as its structure can be modified to create compounds with potential therapeutic effects. Researchers often employ it in the synthesis of alkaloids and other nitrogen-containing heterocycles, which are common in many drugs. Additionally, its protective group properties make it useful in multi-step synthetic processes, ensuring specific functional groups remain unaffected during reactions. Its application extends to the study of biochemical pathways and the development of new medicinal agents targeting various diseases.
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