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

≥95%

Reagent Code: #85539
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CAS Number 622867-52-1

science Other reagents with same CAS 622867-52-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.33 g/mol
Formula C₁₅H₂₁NO₃
badge Registry Numbers
MDL Number MFCD12408124
thermostat Physical Properties
Boiling Point 403.7±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in the pharmaceutical industry. It serves as a key building block in the development of various biologically active compounds, including potential drug candidates. Its structure is often exploited in the synthesis of tetrahydroisoquinoline derivatives, which are known for their diverse pharmacological properties, such as antitumor, antiviral, and central nervous system activities. Additionally, the presence of the tert-butyl group and hydroxylmethyl functionality makes it a versatile reagent for further chemical modifications, enabling the creation of novel compounds with tailored properties for research and therapeutic applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,322.00
inventory 1g
10-20 days ฿44,901.00
inventory 250mg
10-20 days ฿17,847.00

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tert-Butyl 6-(hydroxymethyl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
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This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in the pharmaceutical industry. It serves as a key building block in the development of various biologically active compounds, including potential drug candidates. Its structure is often exploited in the synthesis of tetrahydroisoquinoline derivatives, which are known for their diverse pharmacological properties, such as antitumor, antiviral, and central nervous system activities. Additionally, the presence of the tert-butyl group and hydroxylmethyl functionality makes it a versatile reagent for further chemical modifications, enabling the creation of novel compounds with tailored properties for research and therapeutic applications.
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