CAS 37942-07-7
:3,5-Di-terc-butilsalicilaldehído
Descripción:
3,5-Di-terc-butilsalicilaldehído es un compuesto orgánico caracterizado por su estructura aromática, que presenta un grupo salicilaldehído con dos grupos tert-butilo posicionados en las posiciones 3 y 5 del anillo bencénico. Este compuesto suele aparecer como un líquido o sólido de color amarillo pálido a incoloro, dependiendo de la temperatura y la pureza. Es conocido por su distintivo olor aromático y es soluble en disolventes orgánicos como el etanol y el éter, pero tiene una solubilidad limitada en agua debido a sus grupos tert-butilo hidrofóbicos. La presencia del grupo funcional aldehído contribuye a su reactividad, permitiéndole participar en varias reacciones químicas, incluyendo condensación y oxidación. Además, 3,5-Di-terc-butilsalicilaldehído exhibe propiedades antioxidantes, lo que lo hace de interés en diversas aplicaciones, incluyendo farmacéuticos y ciencia de materiales. Su estabilidad y reactividad pueden verse influenciadas por factores ambientales como la temperatura y el pH, que son consideraciones importantes en su manejo y almacenamiento.
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
Clave 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 más sinónimos
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Encontrado 7 productos.
3,5-Di-tert-butylsalicylaldehyde
CAS:Fórmula:C15H22O2Pureza:>98.0%(GC)Forma y color: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%Forma y color:Crystalline solid or powder, White to cream to yellowPeso molecular:234.343,5-Di-tert-butyl-2-hydroxybenzaldehyde
CAS:Fórmula:C15H22O2Pureza:98%Forma y color:SolidPeso molecular:234.33403,5-Bis(tert-butyl)-2-hydroxybenzaldehyde
CAS:<p>3,5-Bis(tert-butyl)-2-hydroxybenzaldehyde</p>Fórmula:C15H22O2Pureza:98%Forma y color: 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%Forma y color:Off-White PowderPeso molecular:234.33 g/mol3,5-Di-tert-butyl-2-hydroxybenzaldehyde
CAS:Fórmula:C15H22O2Pureza:97%Forma y color:Solid, Crystalline PowderPeso molecular:234.3393,5-Di-t-butyl-2-hydroxybenzaldehyde
CAS:Producto 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:C15H22O2Forma y color:NeatPeso molecular:234.33






