| Identification | More | [Name]
Indole-5-carboxaldehyde | [CAS]
1196-69-6 | [Synonyms]
1H-INDOLE-5-CARBALDEHYDE
1H-INDOLE-5-CARBOXALDEHYDE
5-FORMYLINDOLE
5-INDOLE ALDEHYDE
INDOLE-5-ALDEHYDE
INDOLE-5-CARBALDEHYDE
INDOLE-5-CARBOXALDEHYDE
5-Formyl-1H-indole
1H-Indole-5-carboxaldehyde (9CI)
INDOLE-5-CARBOXYALDEHYDE
INDOLE-5-CARBOXALDEHYDE (5-FORMYLINDOLE)
1H-INDOLE-5-CARBALDEHYDEINDOLE-5-CARBOXALDEHYDE
Indole-5-Carboxadehyde
INDOLE-5-CARBOXALDEHYDE, 98+% | [EINECS(EC#)]
627-955-1 | [Molecular Formula]
C9H7NO | [MDL Number]
MFCD02093664 | [Molecular Weight]
145.16 | [MOL File]
1196-69-6.mol |
| Chemical Properties | Back Directory | [Appearance]
Red Crystalline Powder | [Melting point ]
100-103 °C(lit.) | [Boiling point ]
339.1±15.0 °C(Predicted) | [density ]
1.278±0.06 g/cm3(Predicted) | [storage temp. ]
Keep Cold | [form ]
Powder | [pka]
16.14±0.30(Predicted) | [color ]
Orange or tan | [Water Solubility ]
Insoluble in water. | [Sensitive ]
Air Sensitive | [CAS DataBase Reference]
1196-69-6(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 .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [WGK Germany ]
3
| [Hazard Note ]
Irritant/Keep Cold | [HazardClass ]
IRRITANT | [HS Code ]
29339900 |
| Hazard Information | Back Directory | [Chemical Properties]
Red Crystalline Powder | [Uses]
Indole-5-carboxaldehyde is used as a reactant in preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents; and in synthesis of para-para stilbenophanes by McMurry coupling. It is also used as a reactant in stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes and in structure-based drug design of aurora kinase A inhibitors. | [Uses]
Reactant in preparation of curcumin derivatives as anti-proliferative & anti-inflammatory agents 1 Reactant in preparation of analogs of botulinum neurotoxin serotype A protease inhibitors 2 Reactant in stereoselective synthesis of dibenzylideneacetone derivatives as β-amyloid imaging probes 3 Reactant in synthesis of para-para stilbenophanes by McMurry coupling 4 Reactant in stereoselective synthesis of heteroaromatic (E)-α,β-unsaturated ketones from aldehydes 5 Reactant in structure-based drug design of aurora kinase A inhibitors. |
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