Substance
ID:325940
Names and Identifiers
Synonyms
1-甲基吲哚-3-甲酸1-Methylindole-3-carboxylic acid
IUPAC name
1-methyl-1H-indole-3-carboxylic acid
IUPAC Traditional name
1-methylindole-3-carboxylic acid
Properties
Safety Information
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
European Hazard Symbols
Irritant (Xi)GHS Hazard statements
H315-H319-H335
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Risk Statements
36/37/38
MSDS Link
Safety Statements
26-36
German water hazard class
3
GHS Signal Word
Warning
GHS Precautionary statements
P261-P305+P351+P338
Physical Property
Melting Point
197-200 °C (dec.)(lit.)
Product Information
Empirical Formula (Hill Notation)
C10H9NO2
Purity
97%
Molecule Details
Packaging
1, 5 g in glass bottle
Application
• Reactant for preparation of bisindolyl pyrimidinones analogs of PKC inhibitor LY3335311
• Reactant for preparation of (heteroaryl)(carboxamido)arylpyrrole derivatives as Cdc7 kinase inhibitors, antitumor and antiproliferative agents2
• Reactant for preparation of (pyrrolidinylmethoxy)cyclohexanecarboxylic acids as antigen-4 (VLA-4) antagonists3
• Reactant for preparation of EphB3 receptor tyrosine kinase inhibitors4
• Reactant for preparation of pyrazolodiazepine derivatives as human P2X7 receptor antagonists5
• Reactant for preparation of potent nonpeptidic urotensin II receptor agonists6
• Reactant for preparation of pyrrolizidine esters, amides, and ureas as 5-HT4 receptor ligands7
1, 5 g in glass bottle
Application
• Reactant for preparation of bisindolyl pyrimidinones analogs of PKC inhibitor LY3335311
• Reactant for preparation of (heteroaryl)(carboxamido)arylpyrrole derivatives as Cdc7 kinase inhibitors, antitumor and antiproliferative agents2
• Reactant for preparation of (pyrrolidinylmethoxy)cyclohexanecarboxylic acids as antigen-4 (VLA-4) antagonists3
• Reactant for preparation of EphB3 receptor tyrosine kinase inhibitors4
• Reactant for preparation of pyrazolodiazepine derivatives as human P2X7 receptor antagonists5
• Reactant for preparation of potent nonpeptidic urotensin II receptor agonists6
• Reactant for preparation of pyrrolizidine esters, amides, and ureas as 5-HT4 receptor ligands7
Molecular Spectra
No Data Available
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References
No Data Available
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