CAS 480-67-1
:Ácido 2,6-diidroxi-4-metilbenzóico
Descrição:
Ácido 2,6-diidroxi-4-metilbenzóico, também conhecido como ácido gentísico, é um composto aromático caracterizado pela presença de dois grupos hidroxila e um grupo ácido carboxílico ligados a um anel benzênico. Sua fórmula molecular é C8H8O4, e apresenta um grupo metila na posição para em relação ao ácido carboxílico. Este composto é tipicamente um sólido cristalino branco a amarelo pálido que é solúvel em água e solventes orgânicos, refletindo seus grupos funcionais polares. Ácido 2,6-diidroxi-4-metilbenzóico exibe propriedades antioxidantes e é de interesse em vários campos, incluindo farmacêuticos e bioquímica, devido às suas potenciais aplicações na síntese de corantes, bem como seu papel nas vias metabólicas. O composto pode sofrer várias reações químicas, incluindo esterificação e oxidação, tornando-o versátil na síntese orgânica. Seu número CAS, 480-67-1, é usado para identificação em bancos de dados químicos e contextos regulatórios.
Fórmula: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)
Chave InChI:InChIKey=YBZAVRDNSPUMFK-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=C(O)C=C(C)C=C1O
Sinónimos:- 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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100
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90
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95
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6 produtos.
2,6-Dihydroxy-4-methylbenzoic Acid
CAS:Fórmula:C8H8O4Cor e Forma:White to Almost white powder to crystalPeso molecular:168.152,6-Dihydroxy-4-methylbenzoic acid
CAS:2,6-Dihydroxy-4-methylbenzoic acidFórmula:C8H8O4Pureza:≥95%Cor e Forma: off-white powderPeso molecular: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>Fórmula:C8H8O4Pureza:Min. 98 Area-%Cor e Forma:SolidPeso molecular: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>Fórmula:C16H16O8•CuPureza:Min. 95%Peso molecular:399 g/mol2,6-Dihydroxy-4-methylbenzoic acid monohydrate
CAS:Fórmula:C8H10O5Pureza:99.0%Cor e Forma:SolidPeso molecular:186.163




