1-Methylindole-2-carboxylic Acid

≥98.0%(GC)

Reagent Code: #206041
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CAS Number 16136-58-6

science Other reagents with same CAS 16136-58-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.18 g/mol
Formula C₁₀H₉NO₂
badge Registry Numbers
MDL Number MFCD00005801
thermostat Physical Properties
Melting Point 212-213°C dec. (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used in pharmaceutical research as an intermediate for synthesizing bioactive molecules, particularly in the development of indole-based drug candidates. Shows potential in the study of neurological and inflammatory pathways due to the indole scaffold's affinity for various receptors. Also employed in agrochemical research for designing new pesticides with improved selectivity. Its carboxylic acid group allows for easy derivatization, making it valuable in combinatorial chemistry and structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿156.00
inventory 5g
10-20 days ฿680.00
inventory 25g
10-20 days ฿2,810.00

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1-Methylindole-2-carboxylic Acid
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Used in pharmaceutical research as an intermediate for synthesizing bioactive molecules, particularly in the development of indole-based drug candidates. Shows potential in the study of neurological and inflammatory pathways due to the indole scaffold's affinity for various receptors. Also employed in agrochemical research for designing new pesticides with improved selectivity. Its carboxylic acid group allows for easy derivatization, making it valuable in combinatorial chemistry and structure-activity r

Used in pharmaceutical research as an intermediate for synthesizing bioactive molecules, particularly in the development of indole-based drug candidates. Shows potential in the study of neurological and inflammatory pathways due to the indole scaffold's affinity for various receptors. Also employed in agrochemical research for designing new pesticides with improved selectivity. Its carboxylic acid group allows for easy derivatization, making it valuable in combinatorial chemistry and structure-activity relationship studies.

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