338800-72-9

Basic information

• Product Name: (1S,2S,5R)-1-[N,N-Bis(2-hydroxyethyl)aminomethyl]-1-hydroxy-5-methyl-2-(1-methylethyl)cyclohexane
• CAS NO: 338800-72-9
• Molecular Weight: 273.416
• Mol File: 338800-72-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2S,5R)-1-[N,N-Bis(2-hydroxyethyl)aminomethyl]-1-hydroxy-5-methyl-2-(1-methylethyl)cyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S,5R)-1-[N,N-Bis(2-hydroxyethyl)aminomethyl]-1-hydroxy-5-methyl-2-(1-methylethyl)cyclohexane(338800-72-9)
• EPA Substance Registry System: (1S,2S,5R)-1-[N,N-Bis(2-hydroxyethyl)aminomethyl]-1-hydroxy-5-methyl-2-(1-methylethyl)cyclohexane(338800-72-9)

Safety Data

• Hazardous Substances Data: 338800-72-9(Hazardous Substances Data)

Upstream product

• 111-42-2 2,2'-iminobis[ethanol] 
• 184178-86-7 (1S,4S,7R)-4-isopropyl-7-methyl-1-oxaspiro[2.5]octane 

Relevant articles and documents

Synthesis and structure of chiral silatranes derived from terpenes

Starting with the chiral pool compounds (-)-menthone, (-)-limonene, (-)-β-pinene, and (-)-carvone, new homochiral triethanolamine derivatives were obtained and converted to chiral silatranes. These silatraries were characterized by crystal structure analyses and NMR techniques. Conformational analyses in the solid state and in solution show that the chiral terpene residues determine the direction of the ring puckering of the silatrane moiety.