73441-43-7

Usage

Uses

Used in Pharmaceutical Industry:
Benzenemethanamine, alpha-methyl-4-(1-methylethyl)(9CI) is utilized as a precursor in the synthesis of various drugs, playing a crucial role in the development of medicinal compounds.
Used in Organic Chemistry Experiments:
Benzenemethanamine, alpha-methyl-4-(1-methylethyl)(9CI) also serves as a reagent in organic chemistry, aiding in various experimental procedures and reactions.

InChI:InChI=1/C11H17N/c1-8(2)10-4-6-11(7-5-10)9(3)12/h4-9H,12H2,1-3H3

Upstream product

• 5359-04-6 1-(4-(prop-1-en-2-yl)phenyl)ethan-1-one 
• 98405-01-7 1-(4-Isopropylphenyl)-ethylamine*mandelic acid salt 
• 98405-01-7 1-(4-Isopropylphenyl)-ethylamine*mandelic acid 
• 98571-16-5 1-(4-Isopropyl-phenyl)-ethylamine; compound with (E)-3-phenyl-acrylic acid 
• 98571-16-5 1-(4-Isopropyl-phenyl)-ethylamine; compound with (E)-3-phenyl-acrylic acid 
• 645-13-6 4-isopropylacetophenone 

Downstream Products

• 73441-45-9 N,N-dimethyl-1-(4-isopropylphenyl)-ethylamine 
• 98571-19-8 (S)-1-(4-Isopropyl-phenyl)-ethylamine; compound with 2-hydroxy-succinic acid 
• 98571-16-5 1-(4-Isopropyl-phenyl)-ethylamine; compound with (E)-3-phenyl-acrylic acid 
• 98571-16-5 1-(4-Isopropyl-phenyl)-ethylamine; compound with (E)-3-phenyl-acrylic acid 
• 98405-01-7 1-(4-Isopropylphenyl)-ethylamine*mandelic acid salt 
• 98405-01-7 1-(4-Isopropylphenyl)-ethylamine*mandelic acid 

Relevant academic research and scientific papers

Catalytic asymmetric oxidative carbonylation-induced kinetic resolution of sterically hindered benzylamines to chiral isoindolinones

A highly enantioselective kinetic resolution of sterically hindered benzylamines has been achieved for the first time through transition-metal-catalyzed oxidative carbonylation, in which the new KR strategy offered a new approach to afford chiral isoindolinones (er up to 97?:?3) and the origin of chemoselectivity and stereoselectivity was confirmed by density functional theory (DFT) calculations.

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):

Isopropylbenzene derivatives

Isopropylbenzene derivatives having the general formula: STR1 in which: R1 to R4 independently represent a hydrogen atom or a lower alkyl group having up to 4 carbon atoms, X? represents COO? or SO3s