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Thermo Scientific Chemicals
5-Methylindole-2-carboxylic acid, 99%
CAS: 10241-97-1 | C10H9NO2 | 175.19 g/mol
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化學識別
CAS10241-97-1
IUPAC Name5-methyl-1H-indole-2-carboxylic acid
Molecular FormulaC10H9NO2
InChI KeyDAITVOCMWPNFTL-UHFFFAOYSA-N
SMILESCC1=CC=C2NC(=CC2=C1)C(O)=O
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規格
規格表
規格表Appearance (Color)Yellow or cream to pale brown
FormPowder
Assay (Aqueous acid-base Titration)≥98.5 to ≤101.5%
Assay (HPLC)≥98.5%
5-Methylindole-2-carboxylic acid is a compound used in the synthesis of Pin1 inhibitors as potential antitumor agents. reactant in preparation of Pin1 inhibitors as potential antitumor agents reactant in preparation of non-imidazole human histamine H4 receptor antagonists
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
5-Methylindole-2-carboxylic acid is a compound used in the synthesis of Pin1 inhibitors as potential antitumor agents. reactant in preparation of Pin1 inhibitors as potential antitumor agents reactant in preparation of non-imidazole human histamine H4 receptor antagonists
Solubility
Soluble in ethanol (50 mg/ml). Insoluble in water.
Notes
Keep container tightly closed. Store away from oxidizing agents.
5-Methylindole-2-carboxylic acid is a compound used in the synthesis of Pin1 inhibitors as potential antitumor agents. reactant in preparation of Pin1 inhibitors as potential antitumor agents reactant in preparation of non-imidazole human histamine H4 receptor antagonists
Solubility
Soluble in ethanol (50 mg/ml). Insoluble in water.
Notes
Keep container tightly closed. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- Anja Lüth.; Werner Löwe. Syntheses of 4-(indole-3-yl)quinazolines - A new class of epidermal growth factor receptor tyrosine kinase inhibitors. European Journal of Medicinal Chemistry. 2008, 43 (7), 1478-1488.
- Takumi Tanaka.; Yoshihiro Minematsu.; Christopher F. Reilly.; James Travis.; James C. Powers. Human leukocyte cathepsin G. Subsite mapping with 4-nitroanilides, chemical modification, and effect of possible cofactors. Biochemistry. 1985, 24 (8), 2040-2047.