1-Pentyl-1H-indole-3-carboxylic acid

95%

Reagent Code: #226302
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CAS Number 727421-73-0

science Other reagents with same CAS 727421-73-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.29 g/mol
Formula C₁₄H₁₇NO₂
badge Registry Numbers
MDL Number MFCD05859192
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used primarily as a synthetic intermediate in organic chemistry research, particularly in the development of indole-based compounds. It serves as a building block for pharmaceuticals and bioactive molecules due to the indole scaffold’s prevalence in medicinal chemistry. Its carboxylic acid functional group allows for easy derivatization, enabling the synthesis of amides, esters, and other derivatives for structure-activity relationship studies. Commonly employed in the preparation of cannabinoid receptor ligands and related psychoactive substance analogs for forensic and pharmacological research. Also utilized in analytical laboratories as a reference standard for detecting and identifying synthetic cannabinoids in biological samples.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿143.00
inventory 250mg
10-20 days ฿214.50
inventory 1g
10-20 days ฿808.50
inventory 5g
10-20 days ฿3,074.50

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1-Pentyl-1H-indole-3-carboxylic acid
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Used primarily as a synthetic intermediate in organic chemistry research, particularly in the development of indole-based compounds. It serves as a building block for pharmaceuticals and bioactive molecules due to the indole scaffold’s prevalence in medicinal chemistry. Its carboxylic acid functional group allows for easy derivatization, enabling the synthesis of amides, esters, and other derivatives for structure-activity relationship studies. Commonly employed in the preparation of cannabinoid receptor

Used primarily as a synthetic intermediate in organic chemistry research, particularly in the development of indole-based compounds. It serves as a building block for pharmaceuticals and bioactive molecules due to the indole scaffold’s prevalence in medicinal chemistry. Its carboxylic acid functional group allows for easy derivatization, enabling the synthesis of amides, esters, and other derivatives for structure-activity relationship studies. Commonly employed in the preparation of cannabinoid receptor ligands and related psychoactive substance analogs for forensic and pharmacological research. Also utilized in analytical laboratories as a reference standard for detecting and identifying synthetic cannabinoids in biological samples.

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