107398-14-1

Basic information

• Product Name: L-menthyl (3R)-1-iriden-7-oate
• CAS NO: 107398-14-1
• Molecular Weight: 306.489
• Mol File: 107398-14-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: L-menthyl (3R)-1-iriden-7-oate(CAS DataBase Reference)
• NIST Chemistry Reference: L-menthyl (3R)-1-iriden-7-oate(107398-14-1)
• EPA Substance Registry System: L-menthyl (3R)-1-iriden-7-oate(107398-14-1)

Safety Data

• Hazardous Substances Data: 107398-14-1(Hazardous Substances Data)

Upstream product

• 2216-51-5 (-)-menthol 

Downstream Products

• 93221-57-9 [(1R,3S)-3-((R)-2-Benzyloxy-1-methyl-ethyl)-1-methyl-2-methylene-cyclopentyl]-((R)-5-isopropyl-2-methyl-cyclopent-1-enyl)-methanone 
• 93178-07-5 (S)-[(1R,3S)-3-((R)-2-Benzyloxy-1-methyl-ethyl)-1-methyl-2-methylene-cyclopentyl]-((R)-5-isopropyl-2-methyl-cyclopent-1-enyl)-methanol 
• 93178-07-5 (R)-[(1R,3S)-3-((R)-2-Benzyloxy-1-methyl-ethyl)-1-methyl-2-methylene-cyclopentyl]-((R)-5-isopropyl-2-methyl-cyclopent-1-enyl)-methanol 
• 107439-86-1 [(2R,5R)-2-[(S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-cyclopent-1-enylmethyl]-5-isopropyl-2-methyl-cyclopent-(Z)-ylidenemethoxy]-trimethyl-silane 
• 107439-87-2 [(2R,5R)-2-[(S)-5-((R)-2-Benzyloxy-1-methyl-ethyl)-2-methyl-cyclopent-1-enylmethyl]-5-isopropyl-2-methyl-cyclopent-(E)-ylidenemethoxy]-trimethyl-silane 
• 107439-84-9 [(S)-[(1R,3S)-3-((R)-2-Benzyloxy-1-methyl-ethyl)-1-methyl-2-methylene-cyclopentyl]-((R)-5-isopropyl-2-methyl-cyclopent-1-enyl)-methoxy]-trimethyl-silane 
• 107439-83-8 [(R)-[(1R,3S)-3-((R)-2-Benzyloxy-1-methyl-ethyl)-1-methyl-2-methylene-cyclopentyl]-((R)-5-isopropyl-2-methyl-cyclopent-1-enyl)-methoxy]-trimethyl-silane 

Relevant articles and documents

Synthetic Photochemistry. XXXIV. Synthetic Strategy of 5-8-5-Membered Tricyclic Higher Terpenoids Based on the Condensation of Two Optically-Active Iridoids, C10-Synthons Obtained from Photo-Cycloadduct of Methyl 2,4-Dioxo-pentanoate-Isoprene, and Its App

One of the photocycloadducts obtained during methyl 2,4-dioxopentanoate to isoprene was converted to optically active iridoids.Using a CrCl2 reductive-couping reaction, proper combinations of two kinds of enantiomeric iridoids, 1-iriden-7-al and 9-benzylo