CAS 37942-07-7
:3,5-Di-terc-butilsalicilaldeído
Descrição:
3,5-Di-terc-butilsalicilaldeído é um composto orgânico caracterizado por sua estrutura aromática, apresentando um grupo salicilaldeído com dois grupos tert-butilo posicionados nas posições 3 e 5 do anel benzênico. Este composto geralmente aparece como um líquido ou sólido de amarelo pálido a incolor, dependendo da temperatura e pureza. É conhecido por seu distinto odor aromático e é solúvel em solventes orgânicos como etanol e éter, mas tem solubilidade limitada em água devido aos seus grupos tert-butilo hidrofóbicos. A presença do grupo funcional aldeído contribui para sua reatividade, permitindo que participe de várias reações químicas, incluindo condensação e oxidação. Além disso, 3,5-Di-terc-butilsalicilaldeído exibe propriedades antioxidantes, tornando-o de interesse em várias aplicações, incluindo farmacêuticos e ciência dos materiais. Sua estabilidade e reatividade podem ser influenciadas por fatores ambientais como temperatura e pH, que são considerações importantes em seu manuseio e armazenamento.
Fórmula:C15H22O2
InChI:InChI=1S/C15H22O2/c1-14(2,3)11-7-10(9-16)13(17)12(8-11)15(4,5)6/h7-9,17H,1-6H3
Chave InChI:InChIKey=RRIQVLZDOZPJTH-UHFFFAOYSA-N
SMILES:C(C)(C)(C)C1=CC(C(C)(C)C)=CC(C=O)=C1O
Sinónimos:- 2-Hydroxy-3,5-bis(tert-butyl)benzaldehyde
- 2-Hydroxy-3,5-di-tert-butylbenzaldehyde
- 3,5-Bis(1,1-dimethylethyl)-2-hydroxy-benzaldehyde
- 3,5-Bis(1,1-dimethylethyl)-2-hydroxybenzaldehyde
- 3,5-Bis(tert-butyl)salicylaldehyde
- 3,5-Bis-tert-butyl-2-hydroxybenzaldehyde
- 3,5-Di-T-Butyl-Salicylaldehyde
- 3,5-Di-Tert-Butyl Salicylaldehyde
- 3,5-Di-t-butyl-2-hydroxybenzaldehyde
- 3,5-Di-t-butylsalicylaldehyde
- 3,5-Di-tert-butylsalicylaldehyde
- 3,5-Di-tert-butylsalicylic aldehyde
- 3,5-Ditert-butyl-2-hydroxybenzaldehyde
- 3,5-tert-Butyl-2-hydroxybenzaldehyde
- Benzaldehyde, 3,5-bis(1,1-dimethylethyl)-2-hydroxy-
- Ver mais sinónimos
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7 produtos.
3,5-Di-tert-butylsalicylaldehyde
CAS:Fórmula:C15H22O2Pureza:>98.0%(GC)Cor e Forma:Light yellow to Yellow to Green powder to crystalPeso molecular:234.343,5-Di-tert-butyl-2-hydroxybenzaldehyde, 99%
CAS:<p>3,5-Di-tert-butyl-2-hydroxybenzaldehyde is used in the synthesis of Mn(III)-salen complex and its diamino precursor 5,6-diamino-5,6-dideoxy-1,2-O-isopropylidene-3-O-methyl--L-idofuranose, chiral Schiff base ligand for an enantioselective copper-catalyzed addition of phenyl acetylene to imines, chira</p>Fórmula:C15H22O2Pureza:99%Cor e Forma:Crystalline solid or powder, White to cream to yellowPeso molecular:234.343,5-Di-tert-butyl-2-hydroxybenzaldehyde
CAS:Fórmula:C15H22O2Pureza:98%Cor e Forma:SolidPeso molecular:234.33403,5-Bis(tert-butyl)-2-hydroxybenzaldehyde
CAS:<p>3,5-Bis(tert-butyl)-2-hydroxybenzaldehyde</p>Fórmula:C15H22O2Pureza:98%Cor e Forma: off white to faint yellow crystalline solidPeso molecular:234.33397g/mol3,5-Di-tert-butyl-2-hydroxy benzaldehyde
CAS:<p>3,5-Di-tert-butyl-2-hydroxy benzaldehyde is a molecule that has been shown to have inhibitory effects on cancer cells. It has been tested in vitro on carcinoma cell lines with promising results and shows the potential to be used as an anticancer agent. 3,5-Di-tert-butyl-2-hydroxy benzaldehyde inhibits the growth of cancer cells by binding to their DNA and preventing the synthesis of proteins. This drug is also effective against bacterial strains such as Escherichia coli, Salmonella typhimurium, Klebsiella pneumoniae, Pseudomonas aeruginosa, and Vibrio cholerae. 3,5-Di-tert-butyl-2-hydroxy benzaldehyde forms hydrogen bonds with nitrogen atoms that are present in the molecules of these bacteria. The intramolecular hydrogen bonding interactions between 3,5-di tert butyl 2 hydroxyben</p>Fórmula:C15H22O2Pureza:Min. 95%Cor e Forma:Off-White PowderPeso molecular:234.33 g/mol3,5-Di-tert-butyl-2-hydroxybenzaldehyde
CAS:Fórmula:C15H22O2Pureza:97%Cor e Forma:Solid, Crystalline PowderPeso molecular:234.3393,5-Di-t-butyl-2-hydroxybenzaldehyde
CAS:Produto Controlado<p>Applications 3,5-Di-t-butyl-2-hydroxybenzaldehyde is a salicylaldehyde derivative with antibacterial activity used in the preparation nickel complexes. 3,5-Di-t-butyl-2-hydroxybenzaldehyde is structurally related to 3,5-di-t-butylcatechol (DTCAT) but is not as potent an activator of rat skeletal muscle ryanodine receptor Ca2+ channel (RyRC).<br>References Tuerkkan, B. et al.: Trans. Met. Chem., 36, 679 (2011); Fusi, F. et al.: Biochem. Biopharmacol., 69, 485 (2005);<br></p>Fórmula:C15H22O2Cor e Forma:NeatPeso molecular:234.33






