960207-08-3

Basic information

• Product Name: (2R,3R)-1-methoxyspirobrassinol (1S,2R,5S)-menthyl ether
• Synonyms: (2R,3R)-1-methoxyspirobrassinol (1S,2R,5S)-menthyl ether
• CAS NO: 960207-08-3
• Molecular Weight: 420.64
• Mol File: 960207-08-3.mol

Chemical Properties

• CAS DataBase Reference: (2R,3R)-1-methoxyspirobrassinol (1S,2R,5S)-menthyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-1-methoxyspirobrassinol (1S,2R,5S)-menthyl ether(960207-08-3)
• EPA Substance Registry System: (2R,3R)-1-methoxyspirobrassinol (1S,2R,5S)-menthyl ether(960207-08-3)

Safety Data

• Hazardous Substances Data: 960207-08-3(Hazardous Substances Data)

Upstream product

• 20747-49-3 (-)-neomenthol 
• 105748-60-5 1-methoxybrassinin 
• 20752-33-4 (1S)-isomenthol 

Downstream Products

• 1351000-37-7 C₁₈H₁₇Cl₂N₃OS₂ 
• 1351000-35-5 C₁₉H₁₈F₃N₃OS₂ 
• 1351000-31-1 C₁₉H₂₁N₃OS₂ 

Relevant articles and documents

Stereoselective synthesis of (R)-(+)-1-methoxyspirobrassinin, (2R,3R)-(-)-1-methoxyspirobrassinol methyl ether and their enantiomers or diastereoisomers

Stereoselective synthesis of cruciferous indole phytoalexin (R)-(+)-1-methoxyspirobrassinin and its unnatural (S)-(-)-enantiomer was achieved by spirocyclization of 1-methoxybrassinin in the presence of (+)- and (-)-menthol and subsequent oxidation of the

Stereoselective synthesis of 1-methoxyspiroindoline phytoalexins and their amino analogues

The stereoselective synthesis of the spiroindoline phytoalexin (R)-(+)-1-methoxyspirobrassinin and its unnatural (S)-(-)-enantiomer were achieved by the bromine-induced spirocyclization of 1-methoxybrassinin using chiral auxiliaries (+)- and (-)-menthol,