6-Hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester

95%

Reagent Code: #196440
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CAS Number 185057-06-1

science Other reagents with same CAS 185057-06-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.32 g/mol
Formula C₁₇H₁₇NO₃
thermostat Physical Properties
Boiling Point 478.6±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.264±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It serves as a building block for isoquinoline-based structures, which are found in certain bioactive molecules and alkaloid derivatives. Its protected carboxylic acid functional group (as benzyl ester) and free hydroxy group allow selective reactions in multi-step organic syntheses, making it valuable in medicinal chemistry for creating potential neuroprotective or neuromodulatory drugs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,410.00
inventory 250mg
10-20 days ฿21,610.00
inventory 1g
10-20 days ฿43,230.00

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6-Hydroxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It serves as a building block for isoquinoline-based structures, which are found in certain bioactive molecules and alkaloid derivatives. Its protected carboxylic acid functional group (as benzyl ester) and free hydroxy group allow selective reactions in multi-step organic syntheses, making it valuable in medicinal chemistry for creating potential neuroprotective or neuromo
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system agents. It serves as a building block for isoquinoline-based structures, which are found in certain bioactive molecules and alkaloid derivatives. Its protected carboxylic acid functional group (as benzyl ester) and free hydroxy group allow selective reactions in multi-step organic syntheses, making it valuable in medicinal chemistry for creating potential neuroprotective or neuromodulatory drugs.
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