76808-14-5

Usage

InChI:InChI=1/C11H17N/c1-7-5-8(2)11(10(4)12)9(3)6-7/h5-6,10H,12H2,1-4H3

Upstream product

• 20173-89-1 1-(2,4,6-trimethylphenyl)ethanimine 
• 2571-52-0 cyanomesitylene 

Downstream Products

• 75326-11-3 N-benzhydrylidene-1-(2,4,6-trimethylphenyl)ethylamine 
• 263351-61-7 [(R)-1-(2,4,6-Trimethyl-phenyl)-ethyl]-carbamic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 263351-60-6 [(S)-1-(2,4,6-Trimethyl-phenyl)-ethyl]-carbamic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 89839-56-5 3,3-(2,2'-biphenylylene)-2-<1-(2,4,6-trimethylphenyl)ethyl>oxaziridine 
• 89839-59-8 N-(9-fluorenylidene)-1-(2,4,6-trimethylphenyl)ethylamine N-oxide 
• 89839-57-6 N-benzhydrylidene-1-(2,4,6-trimethylphenyl)ethylamine N-oxide 
• 89839-58-7 N-<1-(2,4,6-trimethylphenyl)ethylidene>diphenylmethylamine N-oxide 
• 75326-12-4 3,3-diphenyl-2-<1-(2,4,6-trimethylphenyl)ethyl>oxaziridine 
• 263351-63-9 (S)-N-formyl-1-mesitylethylamine 
• 20050-17-3 (1S)-1-(2,4,6-trimethylphenyl)ethanamine 

Relevant academic research and scientific papers

Process for producing optically active 3,3,3-Trifluoro-2-Hydroxy-2-Methylpropionic acid, and salt thereof

There are disclosed are a diastereomer salt of formula (1): a process for producing the same, a process for producing optically active 3,3,3-trifluoro-2-hydroxy-2-methylpropionic acid of formula (2′): a novel optically active amine compound of formula (4): a novel optically active amine compound of formula (8): an imine compound of formula (7) or (11):

A new non-natural chiral auxiliary: Design, synthesis, and resolution of 1-mesitylethylamine and its application in the asymmetric aza-Diels-Alder reaction

1-Mesitylethylamine was designed as a new non-natural chiral auxiliary. Racemic 1-mesitylethylamine could be synthesized in two steps from mesityl cyanide and could be resolved via separation of diastereomeric carbamates derived from (-)-menthyl chlorofor