| Identification | More | [Name]
Indole-4-carboxylic acid | [CAS]
2124-55-2 | [Synonyms]
1H-4-INDOLECARBOXYLIC ACID
1H-INDOLE-4-CARBOXYLIC ACID
4-CARBOXYINDOLE
4-INDOLECARBOXYLIC ACID
INDOLE-4-CARBOXYLIC ACID
RARECHEM AL BE 1201
Indole-4-Carbocylic acid
4-INDOLE CARBOXYLIC ACIDINDOLE-4-CARBOXYLIC ACID
Indole-4-carboxylic acid ,98% | [EINECS(EC#)]
621-279-0 | [Molecular Formula]
C9H7NO2 | [MDL Number]
MFCD00009739 | [Molecular Weight]
161.16 | [MOL File]
2124-55-2.mol |
| Chemical Properties | Back Directory | [Appearance]
Beige powder | [Melting point ]
213-214 °C (lit.) | [Boiling point ]
213-214℃ | [density ]
1.408±0.06 g/cm3(Predicted) | [storage temp. ]
Keep Cold | [form ]
Powder | [pka]
3.90±0.10(Predicted) | [color ]
Beige | [Detection Methods]
HPLC,NMR | [InChI]
InChI=1S/C9H7NO2/c11-9(12)7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,(H,11,12) | [InChIKey]
ROGHUJUFCRFUSO-UHFFFAOYSA-N | [SMILES]
N1C2=C(C(C(O)=O)=CC=C2)C=C1 | [CAS DataBase Reference]
2124-55-2(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HazardClass ]
IRRITANT | [HS Code ]
29339900 |
| Hazard Information | Back Directory | [Chemical Properties]
Beige powder | [Uses]
- 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
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