Methyl 1-oxo-1,2-dihydroisoquinoline-3-carboxylate

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Reagent Code: #208671
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CAS Number 69454-42-8

science Other reagents with same CAS 69454-42-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.19 g/mol
Formula C₁₁H₉NO₃
badge Registry Numbers
MDL Number MFCD10655727
thermostat Physical Properties
Boiling Point 439.7±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of isoquinoline-based bioactive compounds. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting neurological disorders, inflammation, and certain cancers. The compound's ester and ketone functional groups allow for selective chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies in medicinal chemistry. It is also employed in the preparation of enzyme inhibitors and receptor ligands due to its rigid aromatic scaffold.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿539.00
inventory 250mg
10-20 days ฿847.00
inventory 1g
10-20 days ฿2,139.50

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Methyl 1-oxo-1,2-dihydroisoquinoline-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of isoquinoline-based bioactive compounds. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting neurological disorders, inflammation, and certain cancers. The compound's ester and ketone functional groups allow for selective chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies in medicinal ch

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of isoquinoline-based bioactive compounds. Its structure supports the construction of nitrogen-containing heterocycles, which are common in drugs targeting neurological disorders, inflammation, and certain cancers. The compound's ester and ketone functional groups allow for selective chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies in medicinal chemistry. It is also employed in the preparation of enzyme inhibitors and receptor ligands due to its rigid aromatic scaffold.

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