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3934-84-7,MFCD00016518
Catalog No.:AA0037TL

3934-84-7 | 3,4-Dihydroxy-5-methoxybenzoic acid

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250mg
97%
in stock  
$14.00   $10.00
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1g
97%
in stock  
$21.00   $15.00
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10g
97%
in stock  
$198.00   $139.00
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  • Technical Information
  • Properties
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Technical Information
Catalog Number:
AA0037TL
Chemical Name:
3,4-Dihydroxy-5-methoxybenzoic acid
CAS Number:
3934-84-7
Molecular Formula:
C8H8O5
Molecular Weight:
184.1461
MDL Number:
MFCD00016518
SMILES:
COc1cc(cc(c1O)O)C(=O)O
Properties
Computed Properties
 
Complexity:
193  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
2  
XLogP3:
0.7  

Literature

Title: Isolation of methyl syringate as a specific aflatoxin production inhibitor from the essential oil of Betula alba and aflatoxin production inhibitory activities of its related compounds.

Journal: International journal of food microbiology 20120215

Title: Methyl-3-O-methyl gallate and gallic acid from the leaves of Peltiphyllum peltatum: isolation and comparative antioxidant, prooxidant, and cytotoxic effects in neuronal cells.

Journal: Journal of medicinal food 20111101

Title: Complete genome sequence of 'Enterobacter lignolyticus' SCF1.

Journal: Standards in genomic sciences 20111015

Title: Gut metabolites of anthocyanins, gallic acid, 3-O-methylgallic acid, and 2,4,6-trihydroxybenzaldehyde, inhibit cell proliferation of Caco-2 cells.

Journal: Journal of agricultural and food chemistry 20100512

Title: Comparative genome analysis provides insights into the evolution and adaptation of Pseudomonas syringae pv. aesculi on Aesculus hippocastanum.

Journal: PloS one 20100101

Title: Anti-ischemic activity and endothelium-dependent vasorelaxant effect of hydrolysable tannins from the leaves of Rhus coriaria (Sumac) in isolated rabbit heart and thoracic aorta.

Journal: Planta medica 20091101

Title: Synthesis of (-)-epicatechin 3-(3-O-methylgallate) and (+)-catechin 3-(3-O-methylgallate), and their anti-inflammatory activity.

Journal: Chemistry & biodiversity 20090401

Title: Identification of Cabernet Sauvignon anthocyanin gut microflora metabolites.

Journal: Journal of agricultural and food chemistry 20081008

Title: Degradation of 3-O-methylgallate in Sphingomonas paucimobilis SYK-6 by pathways involving protocatechuate 4,5-dioxygenase.

Journal: FEMS microbiology letters 20070901

Title: Biotransformation of gallic acid by Beauveria sulfurescens ATCC 7159.

Journal: Applied microbiology and biotechnology 20070301

Title: Genetic and biochemical investigations on bacterial catabolic pathways for lignin-derived aromatic compounds.

Journal: Bioscience, biotechnology, and biochemistry 20070101

Title: Characterization of the 3-O-methylgallate dioxygenase gene and evidence of multiple 3-O-methylgallate catabolic pathways in Sphingomonas paucimobilis SYK-6.

Journal: Journal of bacteriology 20040801

Title: Antioxidant activity of phenolic and related compounds: a density functional theory study on the O-H bond dissociation enthalpy.

Journal: Redox report : communications in free radical research 20040101

Title: [Studies on chemical constituents in fruits of Tibetan medicine Phyllanthus emblica].

Journal: Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20031001

Title: Molecular mechanisms controlling the rate and specificity of catechol O-methylation by human soluble catechol O-methyltransferase.

Journal: Molecular pharmacology 20010201

Title: Forester SC, et al. Gut metabolites of anthocyanins, gallic acid, 3-O-methylgallic acid, and 2,4,6-trihydroxybenzaldehyde, inhibit cell proliferation of Caco-2 cells. J Agric Food Chem. 2010 May 12;58(9):5320-7.

Title: Forester SC, The anthocyanin metabolites gallic acid, 3-O-methylgallic acid, and 2,4,6-trihydroxybenzaldehyde decrease human colon cancer cell viability by regulating pro-oncogenic signals. Mol Carcinog. 2014 Jun;53(6):432-9.

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Tags:3934-84-7 Molecular Formula|3934-84-7 MDL|3934-84-7 SMILES|3934-84-7 3,4-Dihydroxy-5-methoxybenzoic acid