(1H-Indol-3-yl)acetaldoxime

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Reagent Code: #197883
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CAS Number 2776-06-9

science Other reagents with same CAS 2776-06-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.20 g/mol
Formula C₁₀H₁₀N₂O
badge Registry Numbers
MDL Number MFCD01872524
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as an intermediate in the synthesis of indole-3-acetic acid (IAA), a key auxin-type plant hormone that regulates plant growth processes such as cell elongation, shoot formation, and root development. It serves as an important precursor in the biosynthetic pathway from tryptophan to IAA in certain plants. Additionally, it is utilized in plant biology research to understand hormone production mechanisms and plant responses to environmental stimuli. Due to its structural similarity to natural indole derivatives, it may also be employed in the development of auxin analogs and novel bioactive molecules for agricultural and pharmaceutical applications.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿7,420.00
inventory 50mg
10-20 days ฿27,740.00

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(1H-Indol-3-yl)acetaldoxime
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Used as an intermediate in the synthesis of indole-3-acetic acid (IAA), a key auxin-type plant hormone that regulates plant growth processes such as cell elongation, shoot formation, and root development. It serves as an important precursor in the biosynthetic pathway from tryptophan to IAA in certain plants. Additionally, it is utilized in plant biology research to understand hormone production mechanisms and plant responses to environmental stimuli. Due to its structural similarity to natural indole deriv
Used as an intermediate in the synthesis of indole-3-acetic acid (IAA), a key auxin-type plant hormone that regulates plant growth processes such as cell elongation, shoot formation, and root development. It serves as an important precursor in the biosynthetic pathway from tryptophan to IAA in certain plants. Additionally, it is utilized in plant biology research to understand hormone production mechanisms and plant responses to environmental stimuli. Due to its structural similarity to natural indole derivatives, it may also be employed in the development of auxin analogs and novel bioactive molecules for agricultural and pharmaceutical applications.
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