| Weight | 161.16 g/mol |
|---|---|
| Formula | C9H7NO2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 1 |
Indole-3-carboxylic acid (771-50-6)
Score:
#19 in Medicinal chemistry
,
#1768 in Biochemistry
,
#3882 in Biology
,
#4889 in Chemistry
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- Biosynthesis of Auxin-Induced Ethylene. Effects of Indole-3-Acetic Acid, Benzyladenine and Abscisic Acid on Endogenous Levels of 1-Aminocyclopropane-l-Carboxylic Acid (ACC) and ACC Synthase (Plant and Cell Physiology, 1981)
- Investigation of the inhibition effect of indole-3- carboxylic acid on the copper corrosion in 0.5 m H2SO4 (Corrosion Science, 2008)
- Synthesis of Indole-3-carboxylic Acid Derivatives by Pd(0)-Catalyzed Intramolecular -Arylation of -(2-Iodoanilino) Esters (Journal of Organic Chemistry, 2008)
- The reaction of indole and the indole grignard reagent with phosgene. A facile synthesis of indole-3-carboxylic acid derivatives (Journal of Heterocyclic Chemistry, 1977)
- Synthesis of N-substituted indole-3-carboxylic acid derivatives via Cu(I)-catalyzed intramolecular amination of aryl bromides. (Journal of Organic Chemistry, 2008)
- Palladium-catalyzed annulation of allenes with indole-2-carboxylic acid derivatives: synthesis of indolo[2,3-c]pyrane-1-ones via Ar-I reactivity or C-H functionalization. (Journal of Organic Chemistry, 2012)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C2C(=C1)C(=CN2)C(=O)O
-
InChIKeyKMAKOBLIOCQGJP-UHFFFAOYSA-N
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