246263
Indole-4-carboxylic acid
98%
Synonym(s):
4-Carboxyindole
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About This Item
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Assay
98%
form
powder
mp
213-214 °C (lit.)
SMILES string
OC(=O)c1cccc2[nH]ccc12
InChI
1S/C9H7NO2/c11-9(12)7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,(H,11,12)
InChI key
ROGHUJUFCRFUSO-UHFFFAOYSA-N
Application
- Reactant for preparation of substituted indole derivatives as histamine H3 antagonists
- Reactant for preparation of potent and selective inhibitors of human reticulocyte 15-lipoxygenase-1
- Reactant for preparation of inhibitors of Gli1-mediated transcription in Hedgehog pathway
- Reactant for preparation of pyridinyl carboxylates as SARS-CoV 3CL proinhibitors
- Reactant for preparation of substituted bipiperidinylmethyl amides as CCR3 membrane binding ligands
- Reactant for preparation of indole amide hydroxamic acids as potent inhibitors of histone deacetylases
- Reactant for preparation of 2-[[[4′-chloro-[1,1-biphenyl]-4-yl]thio]methyl]-N-hydroxybutanamide derivatives as specific metalloproteinase
tert-butyl esters of indole and pyrrolecarboylic acids are readily prepared by direct treatment with N,N-dimethylformamide di-tert-butyl acetal (Cat. No. 395005).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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SOLVENT EFFECTS ON THE ELECTRONIC ABSORPTION AND FLUORESCENCE SPECTRA OF INDOLE?4?CARBOXYLIC ACID: PROTOTROPIC EQUILIBRIA IN AQUEOUS SOLUTIONS.
Photochemistry and Photobiology, 45(3), 359-364 (1987)
Synthetic Communications, 34, 3691-3691 (2005)
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