Indole-3-acetic acid derivatives
Indole-3-acetic acid (IAA) derivatives represent a class of plant growth regulators widely used in agriculture and horticulture for their ability to promote root formation, enhance seed germination, and stimulate vegetative growth. These compounds are structurally related to IAA but often exhibit improved efficacy or specificity in various applications. Indole-3-acetic acid derivatives can be synthesized through chemical modifications such as methylation, acetylation, or the introduction of substituents at strategic positions on the indole ring.
These derivatives possess excellent biocompatibility and stability under various environmental conditions, making them suitable for both field and controlled environment applications. They are particularly valuable in improving crop yields and quality by optimizing plant growth and development. Additionally, these substances can be used in tissue culture and genetic transformation processes to enhance plant productivity. Due to their potential benefits, indole-3-acetic acid derivatives have garnered significant interest from researchers and industrialists alike, driving advancements in agricultural technologies and sustainable farming practices.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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1H-Indole-3-acetic acid, 5-methoxy-, ethyl ester | 57000-49-4 | C13H15NO3 |
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Indorenate Hydrochloride | 72318-55-9 | C13H17ClN2O3 |
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Tiplaxtinin | 393105-53-8 | C24H16F3NO4 |
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1H-Indole-3-acetic acid, 4-fluoro-, ethyl ester | 919295-78-6 | C12H12FNO2 |
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2-(5-methoxy-2-methyl-1H-indol-3-yl)acetic acid | 2882-15-7 | C12H13NO3 |
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2-[5-(benzyloxy)-1H-indol-3-yl]acetic acid | 4382-53-0 | C17H15NO3 |
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Methyl 2-(1H-indol-3-yl)acetate | 1912-33-0 | C11H11NO2 |
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2-(6-Bromo-1H-indol-3-yl)acetic acid | 152213-66-6 | C10H8BrNO2 |
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1H-Indole-3-aceticacid, 2-mercapto- | 156135-50-1 | C10H9NO2S |
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1H-Indole-3-aceticacid, 4-ethyl- | 179343-63-6 | C12H13NO2 |
Related Literature
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Ying Li,Weirong Yao,Yunfei Xie,Renjun Pei RSC Adv., 2015,5, 98724-98729
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