1412443-99-2

Basic information

• Product Name: 2-(allyloxy)-6-((1S,2R,3R)-1,2-dihydroxy-3-methylpent-4-en-1-yl)-N,N-diisopropyl-3-methylbenzamide
• Synonyms: 2-(allyloxy)-6-((1S,2R,3R)-1,2-dihydroxy-3-methylpent-4-en-1-yl)-N,N-diisopropyl-3-methylbenzamide
• CAS NO: 1412443-99-2
• Molecular Weight: 389.535
• Mol File: 1412443-99-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(allyloxy)-6-((1S,2R,3R)-1,2-dihydroxy-3-methylpent-4-en-1-yl)-N,N-diisopropyl-3-methylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(allyloxy)-6-((1S,2R,3R)-1,2-dihydroxy-3-methylpent-4-en-1-yl)-N,N-diisopropyl-3-methylbenzamide(1412443-99-2)
• EPA Substance Registry System: 2-(allyloxy)-6-((1S,2R,3R)-1,2-dihydroxy-3-methylpent-4-en-1-yl)-N,N-diisopropyl-3-methylbenzamide(1412443-99-2)

Safety Data

• Hazardous Substances Data: 1412443-99-2(Hazardous Substances Data)

Upstream product

• 22256-43-5 2-methoxy-3-methylbenzoyl chloride 
• 26507-91-5 2-methoxy-3-methylbenzoic acid 
• 52239-62-0 methyl 2-methoxy-3-methylbenzoate 
• 1412443-81-2 2-(allyloxy)-N,N-diisopropyl-3-methylbenzamide 
• 83-40-9 3-methylsalicylic acid 

Relevant articles and documents

Stereoselective Synthesis of Isochromanones by an Asymmetric Ortho-Lithiation Strategy: Synthetic Access to the Isochromanone Core of the Ajudazols

Full details on the design, development, and application of a highly stereoselective strategy for the synthesis of isochromanones are reported. The method is based on an asymmetric ortho lithiation with aldehyde electrophiles and utilizes the chiral memor