(3R)-(-)-3-(1-Methyl-1H-indol-3-yl)butyraldehyde

95%

Reagent Code: #36739
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CAS Number 405873-05-4

science Other reagents with same CAS 405873-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.26 g/mol
Formula C₁₃H₁₅NO
badge Registry Numbers
MDL Number MFCD05664285
thermostat Physical Properties
Melting Point 55.5-59.5℃ (lit.)
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry, where it serves as a key intermediate for developing drugs targeting neurological disorders. Its structure is valuable in creating compounds with potential therapeutic effects on the central nervous system. Additionally, it is employed in research for designing and synthesizing novel indole derivatives, which are explored for their biological activities, including anti-inflammatory and anticancer properties. The compound is also utilized in asymmetric synthesis due to its chiral center, enabling the production of enantiomerically pure substances.

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inventory 1g
10-20 days ฿65,871.00

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(3R)-(-)-3-(1-Methyl-1H-indol-3-yl)butyraldehyde
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Used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry, where it serves as a key intermediate for developing drugs targeting neurological disorders. Its structure is valuable in creating compounds with potential therapeutic effects on the central nervous system. Additionally, it is employed in research for designing and synthesizing novel indole derivatives, which are explored for their biological activities, including anti-inflammatory and anticancer properties.

Used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry, where it serves as a key intermediate for developing drugs targeting neurological disorders. Its structure is valuable in creating compounds with potential therapeutic effects on the central nervous system. Additionally, it is employed in research for designing and synthesizing novel indole derivatives, which are explored for their biological activities, including anti-inflammatory and anticancer properties. The compound is also utilized in asymmetric synthesis due to its chiral center, enabling the production of enantiomerically pure substances.

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