3-(Tetrahydro-2H-pyran-4-yl)indoline-5-carboxylic acid

≥95%

Reagent Code: #65925
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CAS Number 1160248-21-4

science Other reagents with same CAS 1160248-21-4

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scatter_plot Molecular Information
Weight 247.29 g/mol
Formula C₁₄H₁₇NO₃
badge Registry Numbers
MDL Number MFCD12198794
inventory_2 Storage & Handling
Storage room temperature, dry, sealed

description Product Description

This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring both a tetrahydro-2H-pyran ring and an indoline moiety, makes it a valuable intermediate in the creation of molecules targeting central nervous system disorders. Researchers leverage its scaffold to design compounds with potential therapeutic effects for conditions like depression, anxiety, and neurodegenerative diseases. Additionally, its carboxylic acid group allows for further chemical modifications, enabling the development of derivatives with enhanced bioavailability and efficacy. Its role in medicinal chemistry underscores its importance in advancing drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,180.00

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3-(Tetrahydro-2H-pyran-4-yl)indoline-5-carboxylic acid
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This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring both a tetrahydro-2H-pyran ring and an indoline moiety, makes it a valuable intermediate in the creation of molecules targeting central nervous system disorders. Researchers leverage its scaffold to design compounds with potential therapeutic effects for conditions like depression, anxiety, and neurodegenerative diseases. Additionally, its carboxylic

This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring both a tetrahydro-2H-pyran ring and an indoline moiety, makes it a valuable intermediate in the creation of molecules targeting central nervous system disorders. Researchers leverage its scaffold to design compounds with potential therapeutic effects for conditions like depression, anxiety, and neurodegenerative diseases. Additionally, its carboxylic acid group allows for further chemical modifications, enabling the development of derivatives with enhanced bioavailability and efficacy. Its role in medicinal chemistry underscores its importance in advancing drug discovery efforts.

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