493864
2,4,5-Trihydroxybenzaldehyde
99%
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About This Item
Formula condensata:
(HO)3C6H2CHO
Numero CAS:
Peso molecolare:
154.12
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
99%
Punto di fusione
223-225 °C (lit.)
Gruppo funzionale
aldehyde
Stringa SMILE
[H]C(=O)c1cc(O)c(O)cc1O
InChI
1S/C7H6O4/c8-3-4-1-6(10)7(11)2-5(4)9/h1-3,9-11H
WNCNWLVQSHZVKV-UHFFFAOYSA-N
Descrizione generale
2,4,5-Trihydroxybenzaldehyde (2,4,5-THBA) is a tri-substituted benzaldehyde that can be prepared from sesamol. Its free radical-quenching ability, antioxidant bioactivity and cytotoxicity have been assessed. 2,4,5-THBA has been identified as one of the components in the ethyl acetate extract of Beta vulgaris var. cicla seeds. The freezing point, boiling point, density and refractive index of 2,4,5-THBA are 499.65K, 510.61K, 1.3725g/cm3 and 1.6400, respectively.
Applicazioni
2,4,5-Trihydroxybenzaldehyde may be used in the synthesis of:
- 2,4,5-tribenzyloxybenzaldehyde
- 2,4,5-trihydroxybenzaldehyde N-(diphenylmethylene)hydrazine
- 2-hydroxy-4,5-dimethoxybenzaldehyde
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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Benzophenonehydrazone Schiff bases 1-25 were synthesized and their in vitro antiglycation potential has been studied. Out of twenty-five compounds, thirteen showed varying degrees of antiglycation activity with IC50 values ranging between 25.7 - 305 μM, if compared with the standard
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Intermediates for Organic Synthesis, 51-51 (2010)
T H Tseng et al.
Toxicology, 161(3), 179-187 (2001-04-12)
As part of our earlier search for new compounds with improved biological activities including antioxidant, anti-inflammatory, and tumor growth inhibition activities, we synthesized 2,4,5-trihydroxybenzaldehyde (2,4,5-THBA) from commercially available Sesamol. First we examined the free radical-quenching capacity of 2,4,5-THBA, 3,4-dihydroxybenzaldehyde (3,4-DHBA)
Lorenzo Gennari et al.
Phytochemical analysis : PCA, 22(3), 272-279 (2011-02-22)
Beta vulgaris var. cicla (BV) leaves contain chemopreventive compounds that have been investigated for new drug discovery. These compounds belong to the family of the apigenin-glycosides. Since the leaves are seasonal products containing high percentages of water, they are easily
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