CAS 480-67-1
:2,6-Dihydroxy-4-methylbenzoic acid
Description:
2,6-Dihydroxy-4-methylbenzoic acid, also known as gentisic acid, is an aromatic compound characterized by the presence of two hydroxyl groups and a carboxylic acid group attached to a benzene ring. Its molecular formula is C8H8O4, and it features a methyl group at the para position relative to the carboxylic acid. This compound is typically a white to pale yellow crystalline solid that is soluble in water and organic solvents, reflecting its polar functional groups. 2,6-Dihydroxy-4-methylbenzoic acid exhibits antioxidant properties and is of interest in various fields, including pharmaceuticals and biochemistry, due to its potential applications in the synthesis of dyes, as well as its role in metabolic pathways. The compound can undergo various chemical reactions, including esterification and oxidation, making it versatile in organic synthesis. Its CAS number, 480-67-1, is used for identification in chemical databases and regulatory contexts.
Formula:C8H8O4
InChI:InChI=1S/C8H8O4/c1-4-2-5(9)7(8(11)12)6(10)3-4/h2-3,9-10H,1H3,(H,11,12)
InChI key:InChIKey=YBZAVRDNSPUMFK-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=C(O)C=C(C)C=C1O
Synonyms:- 2,6-Dihydroxy-4-Methylbenzoate
- 2,6-Dihydroxy-4-Methylbenzoic Acid Hydrate
- 2,6-Dihydroxy-4-methylbenzoic acid
- 4-Methyl-γ-resorcylic acid
- Benzoic acid, 2,6-dihydroxy-4-methyl-
- p-Orsellinic acid
- γ-Resorcylic acid, 4-methyl-
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Found 6 products.
2,6-Dihydroxy-4-methylbenzoic Acid
CAS:Formula:C8H8O4Color and Shape:White to Almost white powder to crystalMolecular weight:168.152,6-Dihydroxy-4-methylbenzoic acid
CAS:2,6-Dihydroxy-4-methylbenzoic acidFormula:C8H8O4Purity:≥95%Color and Shape: off-white powderMolecular weight:168.15g/mol2,6-Dihydroxy-4-methylbenzoic acid
CAS:<p>2,6-Dihydroxy-4-methylbenzoic acid is a phenolic compound that has been shown to have significant cytotoxicity against cancer cells and may be used in the treatment of various cancers. It is also an endophytic fungus that has been found to produce significant desorption of chloride ions from soil. This compound can also be synthesized by reacting 2,6-dihydroxyphenylacetic acid with methyl iodide or methyl bromide. The reaction system for this synthesis includes concentrated hydrochloric acid, zinc dust, and ethyl acetate. The reaction solution was crystallized in the form of a white solid and the crystals were analyzed by X-ray crystallography to determine their structure. Photocatalytic activity was observed when using 2,6-dihydroxy-4-methylbenzoic acid as an electron donor in a reaction system containing titanium dioxide and hydrogen peroxide as an electron acceptor.</p>Formula:C8H8O4Purity:Min. 98 Area-%Color and Shape:SolidMolecular weight:168.15 g/mol2,6-Dihydroxy-4-methylbenzoic acid copper
CAS:<p>2,6-Dihydroxy-4-methylbenzoic acid copper salt is an organic compound with a skeleton of two benzene rings. The molecule contains a chloride ion coordinated to the copper atom and a methyl group adjacent to the copper atom. This compound has significant cytotoxicity against human cancer cells. It is also an endophytic fungus found in plants that produces ethyl esters of 2,6-dihydroxy-4-methylbenzoic acid copper salt. The chemical structures of this compound are shown in Figure 1 below: Figure 1 The reaction products are 2,6-dichloroquinone and benzoic acid. The reaction solution is a dark red color due to the presence of free quinone groups. This compound has been synthesized using Friedel-Crafts reactions, which were carried out in chloroform and dichloromethane at temperatures ranging from -78°C to room temperature for up to 12</p>Formula:C16H16O8•CuPurity:Min. 95%Molecular weight:399 g/mol2,6-Dihydroxy-4-methylbenzoic acid monohydrate
CAS:Formula:C8H10O5Purity:99.0%Color and Shape:SolidMolecular weight:186.163




