34021-62-0

Basic information

• Product Name: Benzamide, N-(5-hydroxy-1,5-dimethylhexyl)-
• CAS NO: 34021-62-0
• Molecular Formula: C15H23NO2
• Molecular Weight: 249.353
• Mol File: 34021-62-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzamide, N-(5-hydroxy-1,5-dimethylhexyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, N-(5-hydroxy-1,5-dimethylhexyl)-(34021-62-0)
• EPA Substance Registry System: Benzamide, N-(5-hydroxy-1,5-dimethylhexyl)-(34021-62-0)

Safety Data

• Hazardous Substances Data: 34021-62-0(Hazardous Substances Data)

Upstream product

• 372-66-7 heptaminol 
• 98-88-4 benzoyl chloride 
• 543-82-8 1,5-dimethylhexylamine 
• 143565-29-1 5-(2-hydroxy-2-methyl-6-heptyl)-1,3-dibenzylhexahydro-2-oxo-1,3,5-triazine 
• 34021-53-9 N-(1,5-Dimethylhexyl)benzamid 

Relevant articles and documents

Electrochemical Ruthenium-Catalyzed C-H Hydroxylation of Amine Derivatives in Aqueous Acid

The development of an electrochemically driven, ruthenium-catalyzed C-H hydroxylation reaction of amine-derived substrates bearing tertiary C-H bonds is described. The reaction is performed under constant current electrolysis in a divided cell to afford alcohol products in yields comparable to those of our previously reported process, which requires the use of stoichiometric H5IO6 for catalytic turnover. With aqueous acid as solvent, the cathodic electrode reaction simply involves the reduction of protons to evolve hydrogen gas. The optimized protocol offers a convenient, efficient, and atom-economical method for sp3-C-H bond oxidation.

Synthesis of hypusine and other polyamines using dibenzyltriazones for amino protection

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