CAS 37942-07-7
:3,5-Di-tert-butylsalicylaldehyde
- 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-
- See more synonyms
3,5-Di-tert-butylsalicylaldehyde
CAS:Formula:C15H22O2Purity:>98.0%(GC)Color and Shape:Light yellow to Yellow to Green powder to crystalMolecular weight:234.343,5-Di-tert-butyl-2-hydroxybenzaldehyde, 99%
CAS: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
Formula:C15H22O2Purity:99%Color and Shape:Crystalline solid or powder, White to cream to yellowMolecular weight:234.343,5-Di-tert-butyl-2-hydroxybenzaldehyde
CAS:Formula:C15H22O2Purity:98%Color and Shape:SolidMolecular weight:234.33403,5-Bis(tert-butyl)-2-hydroxybenzaldehyde
CAS:3,5-Bis(tert-butyl)-2-hydroxybenzaldehyde
Formula:C15H22O2Purity:98%Color and Shape: off white to faint yellow crystalline solidMolecular weight:234.33397g/mol3,5-Di-tert-butyl-2-hydroxy benzaldehyde
CAS: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
Formula:C15H22O2Purity:Min. 95%Color and Shape:Off-White PowderMolecular weight:234.33 g/mol3,5-Di-tert-butyl-2-hydroxybenzaldehyde
CAS:Formula:C15H22O2Purity:97%Color and Shape:Solid, Crystalline PowderMolecular weight:234.3393,5-Di-t-butyl-2-hydroxybenzaldehyde
CAS:Controlled ProductApplications 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).
References Tuerkkan, B. et al.: Trans. Met. Chem., 36, 679 (2011); Fusi, F. et al.: Biochem. Biopharmacol., 69, 485 (2005);Formula:C15H22O2Color and Shape:NeatMolecular weight:234.33






