6,7-Dimethyl-1H-indole-2-carboxylic acid

97%

Reagent Code: #178610
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CAS Number 383132-15-8

science Other reagents with same CAS 383132-15-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.22 g/mol
Formula C₁₁H₁₁NO₂
badge Registry Numbers
MDL Number MFCD02664418
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Serves as a building block in the development of indole-based drugs, particularly in the design of anti-inflammatory and central nervous system agents. Also employed in research settings for the preparation of fluorescent probes and sensors due to the inherent photophysical properties of the indole scaffold. Its carboxylic acid functionality allows for easy derivatization, making it valuable in combinatorial chemistry and medicinal chemistry for constructing compound libraries.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,130.00
250mg
10-20 days ฿8,630.00
1g
10-20 days ฿21,550.00
5g
10-20 days ฿65,700.00
6,7-Dimethyl-1H-indole-2-carboxylic acid
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Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Serves as a building block in the development of indole-based drugs, particularly in the design of anti-inflammatory and central nervous system agents. Also employed in research settings for the preparation of fluorescent probes and sensors due to the inherent photophysical properties of the indole scaffold. Its carboxylic acid functionality allows for easy derivatization, making it valuable in combinatori

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Serves as a building block in the development of indole-based drugs, particularly in the design of anti-inflammatory and central nervous system agents. Also employed in research settings for the preparation of fluorescent probes and sensors due to the inherent photophysical properties of the indole scaffold. Its carboxylic acid functionality allows for easy derivatization, making it valuable in combinatorial chemistry and medicinal chemistry for constructing compound libraries.

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