78796-73-3

Basic information

• Product Name: (1S,9R,12S)-6-Hydroxy-1-methyl-8,10-dioxo-11-oxa-tricyclo[7.2.1.0^2,7]dodeca-2⁽⁷⁾,3,5-triene-12-carbaldehyde
• Synonyms: (1S,9R,12S)-6-Hydroxy-1-methyl-8,10-dioxo-11-oxa-tricyclo[7.2.1.0^2,7]dodeca-2⁽⁷⁾,3,5-triene-12-carbaldehyde
• CAS NO: 78796-73-3
• Molecular Weight: 246.219
• Mol File: 78796-73-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,9R,12S)-6-Hydroxy-1-methyl-8,10-dioxo-11-oxa-tricyclo[7.2.1.0^2,7]dodeca-2⁽⁷⁾,3,5-triene-12-carbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,9R,12S)-6-Hydroxy-1-methyl-8,10-dioxo-11-oxa-tricyclo[7.2.1.0^2,7]dodeca-2⁽⁷⁾,3,5-triene-12-carbaldehyde(78796-73-3)
• EPA Substance Registry System: (1S,9R,12S)-6-Hydroxy-1-methyl-8,10-dioxo-11-oxa-tricyclo[7.2.1.0^2,7]dodeca-2⁽⁷⁾,3,5-triene-12-carbaldehyde(78796-73-3)

Safety Data

• Hazardous Substances Data: 78796-73-3(Hazardous Substances Data)

Upstream product

• 79-57-2 Oxytetracycline 
• 74-88-4 methyl iodide 

Downstream Products

• 78796-75-5 (1S,9R,12S)-12-Dimethoxymethyl-6-hydroxy-1-methyl-11-oxa-tricyclo[7.2.1.0^2,7]dodeca-2⁽⁷⁾,3,5-triene-8,10-dione 

Relevant articles and documents

AN UNUSUAL REACTION OF TERRAMYCIN WITH METHYL IODIDE

An unusual fragmentation reaction was observed when terramycin is treated with MeI in acetone at room temp.The reaction proceeds with quaternization, loss of trimethylamine, fission of bonds 4a,5 and 12,12a with formation of an aldehydo-lactone derived from rings B, C and D.Additionally some transformations of this lactone are described.