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81779-27-3

81779-27-3 Structure

81779-27-3 Structure
IdentificationBack Directory
[Name]

4-HYDROXY-1H-INDOLE-3-CARBALDEHYDE
[CAS]

81779-27-3
[Synonyms]

Zinc02563745
3-Formyl-4-hydroxy-1H-indole
4-HYDROXYINDOLE-3-CARBALDEHYDE
4-Hydroxyindole-3-carboxaldehyde
4-hydroxy-1H-indol-3-carbaldehyde
4-HYDROXY-1H-INDOLE-3-CARBALDEHYDE
4-Hydroxyindole-3-carboxaldehyde98%
4-HYDROXY-1H-INDOLE-3-CARBOXALDEHYDE
4-Hydroxyindole-3-carboxaldehyde 98%
1H-Indole-3-carboxaldehyde,4-hydroxy-
[Molecular Formula]

C9H7NO2
[MDL Number]

MFCD05864721
[MOL File]

81779-27-3.mol
[Molecular Weight]

161.16
Chemical PropertiesBack Directory
[Melting point ]

198-200 °C
[Boiling point ]

426.3±25.0 °C(Predicted)
[density ]

1.439±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[form ]

solid
[pka]

9.17±0.40(Predicted)
[color ]

Brown
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332-H315-H319-H335
[Precautionary statements ]

P260-P280-P312
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

4-Hydroxy-1H-indole-3-carbaldehyde is a plant metabolite. 4-Hydroxy-1H-indole-3-carbaldehyde can be isolated from Capparis spinosa L. 4-Hydroxy-1H-indole-3-carbaldehyde can be used in the synthesis of fluorescent probe. 4-Hydroxy-1H-indole-3-carbaldehyde can be used in the study of inflammation-related diseases[1][2][3].
[Definition]

ChEBI: 4-hydroxyindole-3-carbaldehyde is a heteroarenecarbaldehyde that is 4-hydroxyindole in which the hydrogen at position 3 has been replaced by a formyl group. It has a role as a plant metabolite. It is a member of hydroxyindoles and a heteroarenecarbaldehyde.
[References]

[1] Haifeng Zhou, et al. Anti-inflammatory effects of caper (Capparis spinosa L.) fruit aqueous extract and the isolation of main phytochemicals. J Agric Food Chem. 2010 Dec 22;58(24):12717-21. DOI:10.1021/jf1034114
[2] Weishan Wang, et al. A single fluorescent probe for imaging ribonucleic acid and sulfur dioxide in living systems and its unique application in tumor and normal cells. J Mater Chem B. 2018 Nov 7;6(41):6607-6614. DOI:10.1039/c8tb02144a
[3] Kdimy A, et al. Phytochemistry, Biological Activities, Therapeutic Potential, and Socio-Economic Value of the Caper Bush (Capparis Spinosa L.). Chem Biodivers. 2022 Oct;19(10):e202200300. DOI:10.1002/cbdv.202200300
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