Home Aldehydes 2,4,6-Trihydroxybenzaldehyde

2,4,6-Trihydroxybenzaldehyde

CAS No.:
487-70-7
Catalog Number:
AG003294
Molecular Formula:
C7H6O4
Molecular Weight:
154.1201
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$19
- +
5g
98%
In Stock USA
United States
$62
- +
10g
98%
In Stock USA
United States
$82
- +
25g
98%
In Stock USA
United States
$150
- +
100g
98%
In Stock USA
United States
$544
- +
Product Description
Catalog Number:
AG003294
Chemical Name:
2,4,6-Trihydroxybenzaldehyde
CAS Number:
487-70-7
Molecular Formula:
C7H6O4
Molecular Weight:
154.1201
MDL Number:
MFCD00003329
IUPAC Name:
2,4,6-trihydroxybenzaldehyde
InChI:
InChI=1S/C7H6O4/c8-3-5-6(10)1-4(9)2-7(5)11/h1-3,9-11H
InChI Key:
BTQAJGSMXCDDAJ-UHFFFAOYSA-N
SMILES:
O=Cc1c(O)cc(cc1O)O
EC Number:
207-663-7
UNII:
I70C45KRO9
NSC Number:
38610
Properties
Complexity:
135  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
154.027g/mol
Formal Charge:
0
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
154.121g/mol
Monoisotopic Mass:
154.027g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
77.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.9  
Literature
Title Journal
Phlorotannins from brown algae (Fucus vesiculosus) inhibited the formation of advanced glycation endproducts by scavenging reactive carbonyls. Journal of agricultural and food chemistry 20120208
Anthocyanin-rich blackberry extract suppresses the DNA-damaging properties of topoisomerase I and II poisons in colon carcinoma cells. Journal of agricultural and food chemistry 20110713
Synthesis, activity testing and molybdenum(VI) complexation of Schiff bases derived from 2,4,6-trihydroxybenzaldehyde investigated as xanthine oxidase inhibitors. ChemMedChem 20110404
Health-Beneficial Phenolic Aldehyde in Antigonon leptopus Tea. Evidence-based complementary and alternative medicine : eCAM 20110101
Phospholipid bilayer formation on a variety of nanoporous oxide and organic xerogel films. Acta biomaterialia 20110101
An update of MALDI-TOF mass spectrometry in lipid research. Progress in lipid research 20110101
Dieckol from Ecklonia cava Regulates Invasion of Human Fibrosarcoma Cells and Modulates MMP-2 and MMP-9 Expression via NF-κB Pathway. Evidence-based complementary and alternative medicine : eCAM 20110101
Gut metabolites of anthocyanins, gallic acid, 3-O-methylgallic acid, and 2,4,6-trihydroxybenzaldehyde, inhibit cell proliferation of Caco-2 cells. Journal of agricultural and food chemistry 20100512
(E)-N'-(2,4,6-Trihydroxy-benzyl-idene)isonicotinohydrazide sesquihydrate. Acta crystallographica. Section E, Structure reports online 20100501
Cellular uptake, stability, visualization by 'Naturstoff reagent A', and multidrug resistance protein 1 gene-regulatory activity of cyanidin in human keratinocytes. Pharmacological research 20100301
Biological activities of polyphenols from grapes. International journal of molecular sciences 20100101
Angiotensin-I-converting enzyme (ACE) inhibitors from marine resources: prospects in the pharmaceutical industry. Marine drugs 20100101
UVA and UVB radiation-induced oxidation products of quercetin. Journal of photochemistry and photobiology. B, Biology 20091202
The bioactivity of dietary anthocyanins is likely to be mediated by their degradation products. Molecular nutrition & food research 20090501
First total synthesis of a polyunsaturated chromone metabolite isolated from the brown algae Zonaria tournefortii. Organic letters 20090205
Identification of Cabernet Sauvignon anthocyanin gut microflora metabolites. Journal of agricultural and food chemistry 20081008
Thermal degradation of anthocyanins and its impact on color and in vitro antioxidant capacity. Molecular nutrition & food research 20071201
Antibacterial activities of phenolic benzaldehydes and benzoic acids against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica. Journal of food protection 20031001
Properties