415688-70-9

Basic information

• Product Name: 2,4-di-tert-butyl-6-(piperidin-1-ylmethyl)phenol
• Synonyms: 2,4-di-tert-butyl-6-(piperidin-1-ylmethyl)phenol
• CAS NO: 415688-70-9
• Molecular Weight: 303.488
• Mol File: 415688-70-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2,4-di-tert-butyl-6-(piperidin-1-ylmethyl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-di-tert-butyl-6-(piperidin-1-ylmethyl)phenol(415688-70-9)
• EPA Substance Registry System: 2,4-di-tert-butyl-6-(piperidin-1-ylmethyl)phenol(415688-70-9)

Safety Data

• Hazardous Substances Data: 415688-70-9(Hazardous Substances Data)

Upstream product

• 110-89-4 piperidine 
• 37942-07-7 3,5-di-tert-butyl-2-hydroxybenzaldehyde 
• 50-00-0 formaldehyd 
• 96-76-4 2,4-di-tert-Butylphenol 

Downstream Products

• 514791-78-7 dichloro(2,4-di-tert-butyl-6-piperidin-1-ylmethyl-phenolato)(η5-cylopentadienyl)titanium 
• 2568-57-2 N-(3-phenyl-2-propynyl)piperidine 
• 1338577-45-9 (2,4-di-tert-butyl-6-(piperidin-1-ylmethyl)phenolate)ZnOBn 

Relevant articles and documents

Synthesis, in silico studies and in vitro evaluation for antioxidant and antibacterial properties of diarylmethylamines: A novel class of structurally simple and highly potent pharmacophore

A series of novel diarylmethylamines were synthesized via simple three component condensation reaction. In vitro antibacterial activity of the synthesized compounds was assessed against Gram-positive and Gram-negative bacteria. Compound 1f containing phen

Imidotungsten(vi) complexes with chelating amino and imino phenolates

The reaction of WOCl4 with 2,4-di-tert-butyl-6-((isopropylamino) methyl)phenol followed by the reaction with phenyl isocyanate leads to the formation of imidotungsten(vi) complex [W(NPh)Cl3(OC 6H3(CH2NH-i-Pr)-2-t-Bu2-4,6)] 4 with a chelating aminophenolate ligand. When the same procedure was applied using aminophenols with bulkier substituents in the amino group, the final product was an unexpected Schiff-base complex [W(NPh)Cl3(OC6H 3(CHNPh)-2-t-Bu2-4,6)] 5, where the ligand is derived from 2,4-di-tert-butyl-6-((phenylimino)methyl)phenol. Complex 5 is also formed in the thermal degradation of 4. On the whole, 5 appears to be formed by a disproportionation of intermediate compounds, which are analogous to complex 4. The solid-state structures of 4 and 5 have been determined by X-ray crystallography whereas the solution structures were studied by 1H and 13C NMR. The Royal Society of Chemistry 2011.

Monocyclopentadienyl phenoxy-imine and phenoxy-amine complexes of titanium and zirconium and their application as catalysts for 1-alkene polymerisation

Deprotonation of the phenol-imines 2-But-6- (RNCH)C6H3OH (R = 2,4,6-Me3C6H2 (1a), C6F5 (1b), C6H11 (1c) and phenolamines leads to the bis(ligand)