144491-18-9

Basic information

• Product Name: Pentanal, 4-methyl-2-(phenylmethoxy)-, (S)-
• CAS NO: 144491-18-9
• Molecular Formula: C13H18O2
• Molecular Weight: 206.285
• Mol File: 144491-18-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Pentanal, 4-methyl-2-(phenylmethoxy)-, (S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Pentanal, 4-methyl-2-(phenylmethoxy)-, (S)-(144491-18-9)
• EPA Substance Registry System: Pentanal, 4-methyl-2-(phenylmethoxy)-, (S)-(144491-18-9)

Safety Data

• Hazardous Substances Data: 144491-18-9(Hazardous Substances Data)

Upstream product

• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 17392-84-6 methyl (2S)-2-hydroxy-4-methylpentanoate 
• 108061-34-3 (S)-methyl 2-benzyloxy-4-methylpentanoate 
• 117175-36-7 (S)-2-(benzyloxy)-4-methylpentan-1-ol 

Downstream Products

• 1251570-88-3 tert-butyl (3S)-3-[(1S)-1-hydroxy-3-methyl-butyl]pyrrolidine-1-carboxylate 
• 143503-67-7 (2S,3S)-3-Benzyloxy-2-hydroxy-5-methyl-hexanenitrile 
• 143516-70-5 (2R,3S)-3-Benzyloxy-2-hydroxy-5-methyl-hexanenitrile 

Relevant articles and documents

Total Syntheses and Configuration Assignments of JBIR-06 and Related Depsipeptides

The first total syntheses of JBIR-06 and two analogous depsipeptides, 12-membered antimycin-class antibiotics, have been accomplished via Shiina macrolactonization. Comparison of the spectroscopic data of the synthesized compounds with those reported for

An enantioselective approach to 3-substituted pyrrolidines: Asymmetric synthesis for pyrrolidine core of serotonin norepinephrine reuptake inhibitors (SNRIs)

A novel and efficient synthetic approach to enantiopure 3-substituted pyrrolidine skeleton from readily available (S)-PMB glycidyl ether as a starting material and its application to the asymmetric synthesis of pyrrolidine core 1 of serotonin norepinephrine reuptake inhibitors (SNRIs) 2 and 3 are described. The synthesis utilizes the organocatalyzed asymmetric Michael addition reaction as key step.