2-(5-Chloro-1H-indol-3-yl)acetic acid

98%

Reagent Code: #41761
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CAS Number 1912-45-4

science Other reagents with same CAS 1912-45-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 209.6290 g/mol
Formula C₁₀H₈ClNO₂
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MDL Number MFCD00130159
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the production of various pharmaceutical agents. Its indole structure makes it valuable for developing compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or anticancer properties. Researchers often employ it in the synthesis of complex molecules for drug discovery and development. Additionally, it can be used in the study of biochemical pathways and receptor interactions, aiding in the understanding of disease mechanisms and the design of targeted therapies. Its chloro and acetic acid functional groups also make it a versatile building block for further chemical modifications.

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Test Parameter Specification
Appearance White to yellow solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,989.00

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2-(5-Chloro-1H-indol-3-yl)acetic acid
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This compound is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the production of various pharmaceutical agents. Its indole structure makes it valuable for developing compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or anticancer properties. Researchers often employ it in the synthesis of complex molecules for drug discovery and development. Additionally, it can be used in the study of biochemical pathways and receptor interactions, aiding in the understanding of disease mechanisms and the design of targeted therapies. Its chloro and acetic acid functional groups also make it a versatile building block for further chemical modifications.
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