CAS 37942-07-7
:3,5-Di-tert-butylsalicylaldehyde
Description:
3,5-Di-tert-butylsalicylaldehyde is an organic compound characterized by its aromatic structure, featuring a salicylaldehyde moiety with two tert-butyl groups positioned at the 3 and 5 positions of the benzene ring. This compound typically appears as a pale yellow to colorless liquid or solid, depending on the temperature and purity. It is known for its distinctive aromatic odor and is soluble in organic solvents such as ethanol and ether, but has limited solubility in water due to its hydrophobic tert-butyl groups. The presence of the aldehyde functional group contributes to its reactivity, allowing it to participate in various chemical reactions, including condensation and oxidation. Additionally, 3,5-Di-tert-butylsalicylaldehyde exhibits antioxidant properties, making it of interest in various applications, including pharmaceuticals and materials science. Its stability and reactivity can be influenced by environmental factors such as temperature and pH, which are important considerations in its handling and storage.
Formula: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
InChI key:InChIKey=RRIQVLZDOZPJTH-UHFFFAOYSA-N
SMILES:C(C)(C)(C)C1=CC(C(C)(C)C)=CC(C=O)=C1O
Synonyms:- 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
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Found 7 products.
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:<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>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:<p>3,5-Bis(tert-butyl)-2-hydroxybenzaldehyde</p>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:<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>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 Product<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>Formula:C15H22O2Color and Shape:NeatMolecular weight:234.33






