143508-85-4

Basic information

• Product Name: (S)-2-(N-3',5'-dibromosalicylidene)-amino-3-methyl-1-butanol
• Synonyms: (S)-2-(N-3',5'-dibromosalicylidene)-amino-3-methyl-1-butanol
• CAS NO: 143508-85-4
• Molecular Weight: 365.065
• Mol File: 143508-85-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)-2-(N-3',5'-dibromosalicylidene)-amino-3-methyl-1-butanol(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(N-3',5'-dibromosalicylidene)-amino-3-methyl-1-butanol(143508-85-4)
• EPA Substance Registry System: (S)-2-(N-3',5'-dibromosalicylidene)-amino-3-methyl-1-butanol(143508-85-4)

Safety Data

• Hazardous Substances Data: 143508-85-4(Hazardous Substances Data)

Upstream product

• 90-59-5 3,5-Dibromosalicylaldehyde 
• 2026-48-4 (S)-valinol 

Relevant articles and documents

Synthesis, characterization and crystal structures of half-sandwich ruthenium complexes with bidentate chiral Schiff-base ligands

Condensation of salicylaldehyde or 5-nitrosalicylaldehyde with (S)-(+)-2-amino-3-methyl-1-butanol in refluxing ethanol afforded the chiral Schiff-base ligands (S)-N-(1-hydroxymethylisobutyl)salicylidene (HL1*) and (S)-N-1-hydroxymethylisobutyl-5-nitrosali

Copper-catalyzed asymmetric oxidation of sulfides

Copper-catalyzed asymmetric sulfoxidation of aryl benzyl and aryl alkyl sulfides, using aqueous hydrogen peroxide as the oxidant, has been investigated. A relationship between the steric effects of the sulfide substituents and the enantioselectivity of th